510(k) K960388 ยท EFQ Gauze/Sponge, Internal
DYNAREX NON-WOVEN SPONGE
| Applicant | Dynarex Corp., Brewster NY, US |
| Decision | Substantially Equivalent, Apr 1, 1996 |
| Received | Jan 26, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960388
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.