Atlas FDA

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

Victoreen, Inc. — Predicate Candidate Screening

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

84 daysmedian FDA review time
240 days90th percentile
40clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K982937MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBERVictoreen, Inc.1998-11-19900
K974112VACUDAP, MODEL 2000, 2001Victoreen, Inc.1998-01-29900
K973960MODEL 37-185Victoreen, Inc.1998-01-14900
K964952VERIDOSE V (FIVE), MODEL NUMBER 37-705Victoreen, Inc.1997-07-212230
K964785VERIDOSE DIODESVictoreen, Inc.1997-06-131960
K971382PRONE BREAST POSITIONING BOARD, MODEL #37-018Victoreen, Inc.1997-06-06840
K952233CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628Victoreen, Inc.1995-06-16350
K940660MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEMVictoreen, Inc.1994-12-092970
K935435NUCLEAR ASSOC 37-08 SER, RAYCAST HP RADIO IMMOB SYSTVictoreen, Inc.1994-07-292610
K941931DIAGNOSTIC X-RAY PATIENT EXPOSURE INDICATORVictoreen, Inc.1994-05-26360
K934549ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELDVictoreen, Inc.1994-02-191500
K935397NUCLEAR ASSOCIATES KNIGHT SR., KNIGHT JR. AND SESAM PORTABLEVictoreen, Inc.1993-12-15360
K932342MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBERVictoreen, Inc.1993-12-132130
K934850NUCLEAR ASSOCIATES PERSONNEL PROTECTIVE SHIELDSVictoreen, Inc.1993-11-22410
K931927VICTOREEN MODEL 530Victoreen, Inc.1993-11-152130
K934548ALL-VUE & GAMMA-VUE VIAL SHIELDSVictoreen, Inc.1993-11-12510
K934362NUCLEAR ASSOCIATES GLASSERSVictoreen, Inc.1993-11-12650
K931657NUCLEAR ASSOCIATES MODEL 34-070 BRACHYTHERAPY CAL.Victoreen, Inc.1993-07-271130
K911340AUTOCOMPVictoreen, Inc.1991-08-261530
K90093237-702 AND 37-703 PC RAINBOWVictoreen, Inc.1990-12-052800
K860260MULTI PURPOSE MODEL 76-903Victoreen, Inc.1986-05-071030
K853754MAGNETIC RESONANCE IMAGING UNIFORMITY/T1 76-901Victoreen, Inc.1986-05-072400
K860100MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902Victoreen, Inc.1986-04-221020
K86046937-701-1 PATIENT DOASE MONITOR WITH DETECTORSVictoreen, Inc.1986-04-16690
K86050436-101 XDS111 XENON DELIVERY/TRAP SYSTEMVictoreen, Inc.1986-04-04520
K853671BEAMSCANVictoreen, Inc.1986-01-101280
K853755ACOUSTICALLY-COUPLED ELECTRONIC PHANTOM 84-410Victoreen, Inc.1985-11-26780
K853756DYNAMIC CARDIAC PHANTOM 74-347Victoreen, Inc.1985-10-29500
K853753DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302Victoreen, Inc.1985-10-02230
K850815RADIOISOTOPE CALIBRATOR MODEL 34-062Victoreen, Inc.1985-08-211740
K851813THERPAC-RADIATION THERAPY TREATMENT PLANNING SYSTEVictoreen, Inc.1985-08-071030
K851812DIGITAL SUBTRACTION ANTIOGRAPHY PHANTOM 76-700/711Victoreen, Inc.1985-06-05400
K851811SLIT CAMERA MODEL 07-624Victoreen, Inc.1985-05-28320
K850813MOBILE LEAD PLASTIC X-RAY BARRIERSVictoreen, Inc.1985-04-10410
K850814MODULAR X-RAY BARRIERSVictoreen, Inc.1985-04-10410
K850816LEAD PLASTIC VIEWING PANELSVictoreen, Inc.1985-04-10410
K837245TRANSPARENT X-RAY COMPENSATION FILTERVictoreen, Inc.1983-04-28510
K810051SELECTRON REMOTE ISOTOPEVictoreen, Inc.1981-02-02340
K792591STRESS TABLE/ERGOMETER SYSTEMVictoreen, Inc.1980-01-04180
K790685POSI-TOTVictoreen, Inc.1979-04-23120

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