# Victoreen, Inc.

- Location (FDA's records): Carle Place, NY
- FDA decisions: 40 (1979–1998): 40 510(k) clearances
- Product codes: IYE (5), KPR (4), LHO (3), EAK (3), KPQ (3), KPT (2), LHN (2), IXY (1), IYI (1), KPX (1), JAQ (1), IXF (1)
- Predicates its devices cite: 6 (4 its own); citations of its devices by later devices: 8 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtec, Inc.: 1 (https://510kreport.com/company/medtec)
- Theta Systems, Inc.: 1 (https://510kreport.com/company/theta-systems)

## Firms that cite its devices most
- Direx Systems Corp.: 1 (https://510kreport.com/company/direx-systems)
- Gammex, Inc.: 1 (https://510kreport.com/company/gammex)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Ptw-New York Corp.: 1 (https://510kreport.com/company/ptw-new-york)

## Its most-cited devices
- K900932: 37-702 and 37-703 PC Rainbow (1990), cited by 1
- K971382: Prone Breast Positioning Board, Model #37-018 (1997), cited by 1
- K940660: Model 37-720 Dual Diode Dosimetry System (1994), cited by 1
- K931927: Victoreen Model 530 (1993), cited by 1
- K853753: Diamentor Patient X-Ray Exposure Indicator 07302 (1985), cited by 1
- K932342: Model 500-6 Radiation Therapy Ionization Chamber (1993), cited by 1

## Recent decisions
- K982937: Model 580-006 Radiation Therapy Ionization Chamber (Nov 19, 1998)
- K974112: Vacudap, Model 2000, 2001 (Jan 29, 1998)
- K973960: MODEL 37-185 (Jan 14, 1998)
- K964952: Veridose V (Five), Model Number 37-705 (Jul 21, 1997)
- K964785: Veridose Diodes (Jun 13, 1997)
- K971382: Prone Breast Positioning Board, Model #37-018 (Jun 6, 1997)
- K952233: Clear-PB Lead Plastic Overhead Barrier 56-628 (Jun 16, 1995)
- K940660: Model 37-720 Dual Diode Dosimetry System (Dec 9, 1994)

Source page: https://510kreport.com/company/victoreen