Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Marquette Electronics, Inc. — Predicate Candidate Screening

82 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

141 daysmedian FDA review time
346 days90th percentile
82clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K971868IMPACT (INFORMING MOBILE PERSONNEL AND CARE TRACKING) PAGER Marquette Electronics, Inc.1997-11-131770
K971683WIRELESS LAN (LOCAL AREA NETWORK) - WIRELESS ETHERNETMarquette Electronics, Inc.1997-10-221680
K972199SIGNAL-AVERAGED HIGH RESOLUTION P WAVE ANALYSISMarquette Electronics, Inc.1997-09-251060
K962547CARDIOSERV PMarquette Electronics, Inc.1997-03-062510
K963120RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEMMarquette Electronics, Inc.1997-02-282000
K962827ALARM DISPLAY UNIT/PAGER-LAN SYSTEM (ADU)Marquette Electronics, Inc.1997-02-242200
K964750EAGLE 4000 PATIENT MONITORMarquette Electronics, Inc.1997-02-21870
K962551CARDIOSERV SMarquette Electronics, Inc.1996-11-191440
K960272EAGLE 3000/3100 PATIENT MONITORMarquette Electronics, Inc.1996-10-022580
K960418EAGLE PATIENT MONITORMarquette Electronics, Inc.1996-10-022470
K961139EAGLE PATIENT MONITOR MODEL 3000/3100Marquette Electronics, Inc.1996-08-091410
K961288BODYTRODEMarquette Electronics, Inc.1996-08-081260
K954852SOLAR 9000 ANESTHESIA INFORMATION MONITORMarquette Electronics, Inc.1996-05-292190
K951130CARDIOSOFT/CARDIOSYSMarquette Electronics, Inc.1996-04-043880
K952474EAGLE 3000 PATIENT MONITORMarquette Electronics, Inc.1995-10-191420
K952101MARQUETTE DEFIB ELECTRODESMarquette Electronics, Inc.1995-09-071260
K935589CENTRA HEART STATIONMarquette Electronics, Inc.1995-08-246440
K941262MARQUETTE DEFIB ELECTRODEMarquette Electronics, Inc.1995-04-204000
K950581SMART ANESTHESIA MULTI-GAS (SAM) MODULEMarquette Electronics, Inc.1995-03-29480
K943977SMART ANESTHESIA MULTI-GAS (SAM) MODULEMarquette Electronics, Inc.1995-03-232190
K950101RAMS (RANDOM ACCESS MASS SPECTROMETER) M-200 RESPIRATORY GASMarquette Electronics, Inc.1995-03-21690
K935394MAC-LAB ELECTROPHYSIOLOGY MODULE OPTIONMarquette Electronics, Inc.1994-10-203460
K943817MARQUETTE ADULT/NEONATAL WRAP SENSORMarquette Electronics, Inc.1994-10-18740
K942752MARQUETTE EAR PROBE SENSORMarquette Electronics, Inc.1994-09-02840
K920790MARQUETTE EAGLE MONITORMarquette Electronics, Inc.1994-04-197880
K934091OXISATMarquette Electronics, Inc.1994-03-152040
K921669MARQUETTE SL SERIES TRANSPORT REMOTE ACQUISITIONMarquette Electronics, Inc.1993-05-073940
K926172SERIES 1500 DEFIBRILLATOR, MODIFICATIONMarquette Electronics, Inc.1993-02-25860
K915073MARQUETTE SV O2 MODULEMarquette Electronics, Inc.1992-12-294170
K921487MARQUETTE SERIES 360 DEFIBRILLATORMarquette Electronics, Inc.1992-12-292740
K922171CENTRA II ANALYSIS SYSTEMMarquette Electronics, Inc.1992-12-282340
K903644SERIES 1500 12-LEAD ANALYSIS OPTIONMarquette Electronics, Inc.1991-12-275010
K912799EAGLE SYSTEMMarquette Electronics, Inc.1991-12-181760
K911662MARQUETTE PEDIATRIC DEFIBRILLATION/PACING PADSMarquette Electronics, Inc.1991-10-101810
K904789SERIES 7000 CARBON DIOXIDE MODULEMarquette Electronics, Inc.1991-05-222110
K902782SERIES 1500 RESPONDERMarquette Electronics, Inc.1991-01-182060
K902176SILVER MACTRODEMarquette Electronics, Inc.1990-09-041120
K901072CENTRALSCOPE 12Marquette Electronics, Inc.1990-08-231690
K902590THREADED PADDLE PAIRS, INTERNAL ADULT PEDI INFANTMarquette Electronics, Inc.1990-07-18360
K900540TRAM PATIENT MONITORMarquette Electronics, Inc.1990-07-171621
K901071PULSE OXIMETRY MODULEMarquette Electronics, Inc.1990-06-191040
K9018847620 REMOTE CENTRAL STATION REPEATERMarquette Electronics, Inc.1990-06-12470
K900598TRAMSCOPE SYSTEMMarquette Electronics, Inc.1990-04-26770
K895801MAC-LAB CARDIAC CATHETERIZATION LABORATORY SYSTEMMarquette Electronics, Inc.1990-04-041880
K895651MARQUETTE 1200 DEFIBRILLATION PADSMarquette Electronics, Inc.1989-12-12830
K895834BABY MAC ELECTROCARDIOGRAPH ELECTRODEMarquette Electronics, Inc.1989-11-03320
K894945NON-INVASIVE BLOOD PRESSURE MODULEMarquette Electronics, Inc.1989-10-26840
K882818SEERMarquette Electronics, Inc.1989-06-223490
K890323MAX-1 (EXERCISE ELECTROCARDIOGRAPH)Marquette Electronics, Inc.1989-06-161440
K891104CD TELEMETRY SYSTEMSMarquette Electronics, Inc.1989-04-19480

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda