# Pgk, Inc.

- Location (FDA's records): Vienna, VA
- FDA decisions: 1 (1998–1998): 1 510(k) clearance
- Product codes: IWJ (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (0 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
- Northern Virginia Radiology and Nuclear Medicine: 1 (https://510kreport.com/company/northern-virginia-radiology-and-nuclear-medicine)
- Bruel & Kjaer: 1 (https://510kreport.com/company/bruel-kjaer)
- Bruel & Kjaer Industri A/S: 1 (https://510kreport.com/company/bruel-kjaer-industri-a-s)

## Recent decisions
- K980997: PGK Device (Modified) (Sep 28, 1998)

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