# Metron U.S., Inc.

- Location (FDA's records): Grand Rapids, MI
- FDA decisions: 4 (1997–1998): 4 510(k) clearances
- Product codes: DPS (1), FRN (1), DQA (1), DRL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Bc Group International, Inc.: 1 (https://510kreport.com/company/bc-group-international)

## Its most-cited devices
- K963190: QA-40M Defibrillator Tester (1997), cited by 1

## Recent decisions
- K982020: Metron QA-Ids I.V. Pump Tester (Sep 30, 1998)
- K973991: Metron QA-510 SPO2 Analyzer (Jan 16, 1998)
- K963190: QA-40M Defibrillator Tester (Jul 1, 1997)
- K963198: PS-41 6M Patient Simulator (Mar 5, 1997)

Source page: https://510kreport.com/company/metron-us