# Percu Surge, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 2 (1998–2001): 2 510(k) clearances
- Product codes: NFA (1), MJN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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
- Edwards Lifesciences, LLC: 1 (https://510kreport.com/company/edwards-lifesciences)
- Boston Scientific Epi: 1 (https://510kreport.com/company/boston-scientific-epi)
- Embol-X, Inc.: 1 (https://510kreport.com/company/embol-x)
- Possis Medical, Inc.: 1 (https://510kreport.com/company/possis-medical)

## Its most-cited devices
- K003992: Percusurge Guardwire Temporary Occlusion and Aspiration System (2001), cited by 3
- K972777: Temporary Occlusion Balloon System (1998), cited by 1

## Recent decisions
- K003992: Percusurge Guardwire Temporary Occlusion and Aspiration System (Jun 1, 2001)
- K972777: Temporary Occlusion Balloon System (Mar 11, 1998)

Source page: https://510kreport.com/company/percu-surge