510(k) K953830 ยท GDY Gauze/Sponge, Internal, X-Ray Detectable
KENSORB
| Applicant | Kentron Health Care, Inc., Hollywood FL, US |
| Decision | Substantially Equivalent, Oct 3, 1995 |
| Received | Aug 16, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953830
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.