# Bc Group International, Inc.

- Location (FDA's records): Oak Grove, MN
- FDA decisions: 2 (2011–2015): 2 510(k) clearances
- Product codes: DRL (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Metron U.S., Inc.: 1 (https://510kreport.com/company/metron-us)
- Fluke Biomedical: 1 (https://510kreport.com/company/fluke-biomedical)

## Firms that cite its devices most
- Netech Corporation: 1 (https://510kreport.com/company/netech)

## Its most-cited devices
- K110192: Defibrillator Analyzer - DA-2006P (2011), cited by 1

## Recent decisions
- K153210: Defibrillator Analyzer Variable Load (Dec 21, 2015)
- K110192: Defibrillator Analyzer - DA-2006P (Feb 8, 2011)

Source page: https://510kreport.com/company/bc-group-international