# Perouse Medical

- Location (FDA's records): France, FR
- FDA decisions: 3 (2012–2013): 3 510(k) clearances
- Product codes: LJT (1), DXC (1), FPA (1)
- Predicates its devices cite: 5 (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
- C.R. Bard, Inc.: 3 (https://510kreport.com/company/cr-bard)
- Terumo Medical Corp.: 1 (https://510kreport.com/company/terumo-medical)
- Laboratoires Perouse: 1 (https://510kreport.com/company/laboratoires-perouse)

## Recent decisions
- K122834: Polysite Implantable Infusion Ports (Dec 11, 2013)
- K123035: Seal One (Nov 28, 2012)
- K120261: PPS PI Pressure Injectable Safety Huber Needle Without Lateral Injection Site, PPS PI Pressure Injectable Safety Huber (May 2, 2012)

Source page: https://510kreport.com/company/perouse-medical