# Fluke Biomedical

- Location (FDA's records): Cleveland, OH
- FDA decisions: 6 (2008–2013): 6 510(k) clearances
- Product codes: DRT (4), DRL (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (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
- Dynatech/Nevada, Inc.: 1 (https://510kreport.com/company/dynatech-nevada)
- Bio-Tek Instruments, Inc.: 1 (https://510kreport.com/company/bio-tek-instruments)

## Firms that cite its devices most
- Bc Group International, Inc.: 1 (https://510kreport.com/company/bc-group-international)
- Seaward Group: 1 (https://510kreport.com/company/seaward-group)

## Its most-cited devices
- K083347: Impulse 7010 Defibrillator Selectable Loads (2008), cited by 1
- K072114: Impulse 6000D/7000DP (2008), cited by 1

## Recent decisions
- K121860: ESA615 (Jan 25, 2013)
- K121722: ESA620 Electrical Safety Analyzer (Oct 11, 2012)
- K110429: Prosim 4, Prosim 6, Prosim 8 (Sep 2, 2011)
- K103336: MPS450 Multiparameter Simulator (Apr 13, 2011)
- K083347: Impulse 7010 Defibrillator Selectable Loads (Dec 24, 2008)
- K072114: Impulse 6000D/7000DP (Jan 28, 2008)

Source page: https://510kreport.com/company/fluke-biomedical