# Genesis Medical Interventional, Inc.

- Location (FDA's records): Redwood City, CA
- FDA decisions: 2 (2004–2009): 2 510(k) clearances
- Product codes: QEW (2)
- Predicates its devices cite: 9 (1 its own); citations of its devices by later devices: 4 (1 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
- Lake Region Mfg., Inc.: 2 (https://510kreport.com/company/lake-region-mfg)
- J-Lloyd Medical, Inc.: 1 (https://510kreport.com/company/j-lloyd-medical)
- LeMaitre Vascular, Inc.: 1 (https://510kreport.com/company/lemaitre-vascular)
- Applied Medical Resources: 1 (https://510kreport.com/company/applied-medical-resources)
- Metamorphic Surgical Devices, LLC: 1 (https://510kreport.com/company/metamorphic-surgical-devices)
- Ideas For Medicine, Inc.: 1 (https://510kreport.com/company/ideas-for-medicine)
- Sunscope Intl., Inc.: 1 (https://510kreport.com/company/sunscope-intl)

## Firms that cite its devices most
- Codman & Shurtleff, Inc.: 1 (https://510kreport.com/company/codman-shurtleff)
- Inari Medical, Inc.: 1 (https://510kreport.com/company/inari-medical)
- Lumen Biomedical, Inc.: 1 (https://510kreport.com/company/lumen-biomedical)

## Its most-cited devices
- K040010: Genesis Medical Interventional F.a.S.T. (Facilitated Aspiration/Suction Thrombectomy) Systems (2004), cited by 3
- K092623: F.a.S.T. System Sed and CXD (2009), cited by 1

## Recent decisions
- K092623: F.a.S.T. System Sed and CXD (Oct 30, 2009)
- K040010: Genesis Medical Interventional F.a.S.T. (Facilitated Aspiration/Suction Thrombectomy) Systems (Jul 19, 2004)

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