510(k) K802798 ยท GDY Gauze/Sponge, Internal, X-Ray Detectable
OPRATEX ABDOMINAL PAD
| Applicant | Secol Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 11, 1980 |
| Received | Nov 4, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802798
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.