Osypka Medical Inc
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Oscor PACE 203H, Dual-Chamber External Pulse Generator The PACE 203H / Model 3085 external recall (Z-2443-2010) | Osypka Medical Inc | 2010-09-21 |
| St. Jude Medical, Model 3085, Dual-Chamber External Pulse Generator The PACE 203H / Model recall (Z-2444-2010) | Osypka Medical Inc | 2010-09-21 |
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Every clearance here is in the API, with alerts when new ones post.