Sanarus Medical Inc
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Sanarus Visica Treatment System (disposable), Model/Product Code: VP-0500 (single) recall (Z-1008-03) | Sanarus Medical Inc | 2003-07-15 |
| Sanarus brand Centrica Rotational Core Biopsy medical device, Model/Product Code: CD-0500 recall (Z-0935-03) | Sanarus Medical Inc | 2003-06-12 |
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Every clearance here is in the API, with alerts when new ones post.