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-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K982937 | MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBER | Victoreen, Inc. | 1998-11-19 | 90 | 0 |
| K974112 | VACUDAP, MODEL 2000, 2001 | Victoreen, Inc. | 1998-01-29 | 90 | 0 |
| K973960 | MODEL 37-185 | Victoreen, Inc. | 1998-01-14 | 90 | 0 |
| K964952 | VERIDOSE V (FIVE), MODEL NUMBER 37-705 | Victoreen, Inc. | 1997-07-21 | 223 | 0 |
| K964785 | VERIDOSE DIODES | Victoreen, Inc. | 1997-06-13 | 196 | 0 |
| K971382 | PRONE BREAST POSITIONING BOARD, MODEL #37-018 | Victoreen, Inc. | 1997-06-06 | 84 | 0 |
| K952233 | CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628 | Victoreen, Inc. | 1995-06-16 | 35 | 0 |
| K940660 | MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM | Victoreen, Inc. | 1994-12-09 | 297 | 0 |
| K935435 | NUCLEAR ASSOC 37-08 SER, RAYCAST HP RADIO IMMOB SYST | Victoreen, Inc. | 1994-07-29 | 261 | 0 |
| K941931 | DIAGNOSTIC X-RAY PATIENT EXPOSURE INDICATOR | Victoreen, Inc. | 1994-05-26 | 36 | 0 |
| K934549 | ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD | Victoreen, Inc. | 1994-02-19 | 150 | 0 |
| K935397 | NUCLEAR ASSOCIATES KNIGHT SR., KNIGHT JR. AND SESAM PORTABLE | Victoreen, Inc. | 1993-12-15 | 36 | 0 |
| K932342 | MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBER | Victoreen, Inc. | 1993-12-13 | 213 | 0 |
| K934850 | NUCLEAR ASSOCIATES PERSONNEL PROTECTIVE SHIELDS | Victoreen, Inc. | 1993-11-22 | 41 | 0 |
| K931927 | VICTOREEN MODEL 530 | Victoreen, Inc. | 1993-11-15 | 213 | 0 |
| K934548 | ALL-VUE & GAMMA-VUE VIAL SHIELDS | Victoreen, Inc. | 1993-11-12 | 51 | 0 |
| K934362 | NUCLEAR ASSOCIATES GLASSERS | Victoreen, Inc. | 1993-11-12 | 65 | 0 |
| K931657 | NUCLEAR ASSOCIATES MODEL 34-070 BRACHYTHERAPY CAL. | Victoreen, Inc. | 1993-07-27 | 113 | 0 |
| K911340 | AUTOCOMP | Victoreen, Inc. | 1991-08-26 | 153 | 0 |
| K900932 | 37-702 AND 37-703 PC RAINBOW | Victoreen, Inc. | 1990-12-05 | 280 | 0 |
| K860260 | MULTI PURPOSE MODEL 76-903 | Victoreen, Inc. | 1986-05-07 | 103 | 0 |
| K853754 | MAGNETIC RESONANCE IMAGING UNIFORMITY/T1 76-901 | Victoreen, Inc. | 1986-05-07 | 240 | 0 |
| K860100 | MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902 | Victoreen, Inc. | 1986-04-22 | 102 | 0 |
| K860469 | 37-701-1 PATIENT DOASE MONITOR WITH DETECTORS | Victoreen, Inc. | 1986-04-16 | 69 | 0 |
| K860504 | 36-101 XDS111 XENON DELIVERY/TRAP SYSTEM | Victoreen, Inc. | 1986-04-04 | 52 | 0 |
| K853671 | BEAMSCAN | Victoreen, Inc. | 1986-01-10 | 128 | 0 |
| K853755 | ACOUSTICALLY-COUPLED ELECTRONIC PHANTOM 84-410 | Victoreen, Inc. | 1985-11-26 | 78 | 0 |
| K853756 | DYNAMIC CARDIAC PHANTOM 74-347 | Victoreen, Inc. | 1985-10-29 | 50 | 0 |
| K853753 | DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302 | Victoreen, Inc. | 1985-10-02 | 23 | 0 |
| K850815 | RADIOISOTOPE CALIBRATOR MODEL 34-062 | Victoreen, Inc. | 1985-08-21 | 174 | 0 |
| K851813 | THERPAC-RADIATION THERAPY TREATMENT PLANNING SYSTE | Victoreen, Inc. | 1985-08-07 | 103 | 0 |
| K851812 | DIGITAL SUBTRACTION ANTIOGRAPHY PHANTOM 76-700/711 | Victoreen, Inc. | 1985-06-05 | 40 | 0 |
| K851811 | SLIT CAMERA MODEL 07-624 | Victoreen, Inc. | 1985-05-28 | 32 | 0 |
| K850813 | MOBILE LEAD PLASTIC X-RAY BARRIERS | Victoreen, Inc. | 1985-04-10 | 41 | 0 |
| K850814 | MODULAR X-RAY BARRIERS | Victoreen, Inc. | 1985-04-10 | 41 | 0 |
| K850816 | LEAD PLASTIC VIEWING PANELS | Victoreen, Inc. | 1985-04-10 | 41 | 0 |
| K837245 | TRANSPARENT X-RAY COMPENSATION FILTER | Victoreen, Inc. | 1983-04-28 | 51 | 0 |
| K810051 | SELECTRON REMOTE ISOTOPE | Victoreen, Inc. | 1981-02-02 | 34 | 0 |
| K792591 | STRESS TABLE/ERGOMETER SYSTEM | Victoreen, Inc. | 1980-01-04 | 18 | 0 |
| K790685 | POSI-TOT | Victoreen, Inc. | 1979-04-23 | 12 | 0 |
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