510(k) K961194 ยท GBW Catheter, Peritoneal
ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN
| Applicant | Sil-Med Corp., Taunton MA, US |
| Decision | Substantially Equivalent, Aug 8, 1996 |
| Received | Mar 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961194
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.