# Physician Industries, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 4 (1995–2004): 4 510(k) clearances
- Product codes: FMF (2), GXD (1), KHR (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 33 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Radionics, A Division of Tyco Healthcare Group LP: 1 (https://510kreport.com/company/radionics-a-division-of-tyco-healthcare-group)
- Radionics, Inc.: 1 (https://510kreport.com/company/radionics)
- Merit Medical Systems, Inc.: 1 (https://510kreport.com/company/merit-medical-systems)
- Professional Medical Services: 1 (https://510kreport.com/company/professional-medical-services)
- Spinal Specialties, Inc.: 1 (https://510kreport.com/company/spinal-specialties)
- B. Braun of America, Inc.: 1 (https://510kreport.com/company/b-braun-of-america)

## Firms that cite its devices most
- Stryker Instruments: 1 (https://510kreport.com/company/stryker-instruments)
- Baylis Medical Co., Inc.: 1 (https://510kreport.com/company/baylis-medical)

## Its most-cited devices
- K033739: Physician Industries' Durameter Syringe (2004), cited by 2

## Recent decisions
- K040565: Physician Industries Radiofrequency Ablation Needle (Jul 22, 2004)
- K033739: Physician Industries' Durameter Syringe (Jul 12, 2004)
- K960248: General Procedure Kit (Apr 12, 1996)
- K954068: General Hygiene Kit (Nov 8, 1995)

Source page: https://510kreport.com/company/physician-industries