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

Honeywell, Inc. · Predicate Candidate Screening

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

34 daysmedian FDA review time
147 days90th percentile
69clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K902230COLORADO COLOR IMAGING RECORDERHoneywell, Inc.1990-06-19330
K863100CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECORHoneywell, Inc.1987-02-031740
K853501HONEYWELL ELECTRONIC VENTILATOR EV-AHoneywell, Inc.1986-04-042270
K855125PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEMHoneywell, Inc.1986-03-26930
K851888APM DISPOS. BLOOD PRESSURE TRANSDUCERHoneywell, Inc.1985-08-06970
K851496ECG MONITOR MODEL RM102Honeywell, Inc.1985-07-241000
K850794PATIENT MONITOR MODEL RM-300Honeywell, Inc.1985-04-18510
K851092PORTABLE DEFIBRILLATOR/MONITOR ED 425Honeywell, Inc.1985-04-10220
K834530EXTENSION BOX EB200Honeywell, Inc.1984-06-011630
K834282ULTRA IMAGER 2000Honeywell, Inc.1984-04-231540
K840167PORTABLE DEFIBRILLATORHoneywell, Inc.1984-02-04190
K831164PATIENT MONITOR CM 135Honeywell, Inc.1983-12-012340
K831696PORTABLE DEFIBRILLATOR MONITOR 74DRKHoneywell, Inc.1983-11-031620
K831817PATIENT MONITOR #RM-100Honeywell, Inc.1983-10-311470
K831818CENTRAL STATION MONITOR CSM-100Honeywell, Inc.1983-10-311470
K832212PATIENT SELECTOR FUNCTION BLOCKHoneywell, Inc.1983-10-141000
K830914EXTERNAL VALVE FUNCTION BLOCKHoneywell, Inc.1983-08-121410
K830566CONVERTER UNIT FOR ECG TRACE DISPLAYHoneywell, Inc.1983-05-25910
K830779PRESSURE FUNCTION BLOCK FOR BLOOD PRESSHoneywell, Inc.1983-05-09590
K822926MODEL LS-85 & MEDEL 1828 LINESCAN VISCOHoneywell, Inc.1982-11-24540
K827408ULTRA IMAGERHoneywell, Inc.1982-10-04680
K822590PRESSURE ISOLATION AMPLIFIER #9813 517Honeywell, Inc.1982-10-04270
K813064TELEMETRY TRANSMITTER & RECEIVERHoneywell, Inc.1981-12-29600
K813125MICRO TRANSDUCER CATHETERSHoneywell, Inc.1981-12-14400
K812667MEDDARS/ULTRA IMAGER RESPIRATION MODULEHoneywell, Inc.1981-10-23320
K812103ESOPHAGEAL MOTILITY APPARATUSHoneywell, Inc.1981-08-13200
K811581ARRHYTHMIA FUNCTION BLOCKHoneywell, Inc.1981-08-13690
K811626MEDDARS/ULTRA IMAGER PULSE/PHON MODULEHoneywell, Inc.1981-07-01220
K810696PHYSIOLOGIC RECORDERHoneywell, Inc.1981-03-27110
K810175NEO NATAL RESPIRATION FUNCTION BLOCKHoneywell, Inc.1981-03-20570
K810174RESPIRATION FUNCTION BLOCKSHoneywell, Inc.1981-03-17540
K810163AM 420 MICROPROCESSORHoneywell, Inc.1981-03-05420
K8101661,2,3 CHANNELL RECORDERS (AR150,AR250,-)Honeywell, Inc.1981-02-25340
K810171PERIPHERAL PULSE FUNCTION BLOCKSHoneywell, Inc.1981-02-25340
K810177PATIENT MONITOR MODEL CM130, 140Honeywell, Inc.1981-02-25340
K810172PRESSURE FUNCTION BLOCKSHoneywell, Inc.1981-02-25340
K810165DUAL TRACE VIDEO MONITOR VM 410Honeywell, Inc.1981-02-25340
K810179DUAL TRACE PATIENT MONITOR 116,118,120Honeywell, Inc.1981-02-25340
K810176ECG FUNCTION BLOCKHoneywell, Inc.1981-02-25340
K810169CENTRAL STATION CONTROLLER AC100/CE100Honeywell, Inc.1981-02-25340
K810178PATIENT MONITOR CM111, 112Honeywell, Inc.1981-02-25340
K810170TREND GRAPH FUNCTION BLOCKHoneywell, Inc.1981-02-25340
K810167SINGLE CHANNELL RECORDER AR110Honeywell, Inc.1981-02-25340
K810168SLAVE MONITORS DC109 & VS109Honeywell, Inc.1981-02-25340
K810164VC 430 VIDEO CONVERTERHoneywell, Inc.1981-02-25340
K810237PORTABLE, BATTERY OPERATED DEFIBRILLATORHoneywell, Inc.1981-02-19220
K810263MICROPROCESSOR CONTROLLED ELECTROCARDIOHoneywell, Inc.1981-02-19200
K810173TEMPERATURE FUNCTION BLOCKHoneywell, Inc.1981-02-02110
K800553ULTRA IMAGERHoneywell, Inc.1980-07-211320
K792677DATABASE MANAGEMENT & REPORTING SYSTEMHoneywell, Inc.1980-01-0480

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