510(k) K130900 ยท FMF Syringe, Piston
EVICEL APPLICATION DEVICE
| Applicant | Ethicon Inc (On Behalf of Omrix Biopharaceuticals, Somerville NJ, US |
| Decision | Substantially Equivalent, Aug 13, 2013 |
| Received | Apr 1, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130900
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.