510(k) K920355 ยท GDY Gauze/Sponge, Internal, X-Ray Detectable
SPECIALTY SPONGES
| Applicant | Ultracell Medical Technologies, Inc., North Stonington CT, US |
| Decision | Substantially Equivalent, Aug 6, 1992 |
| Received | Jan 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920355
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.