510(k) K780718 ยท GDY Gauze/Sponge, Internal, X-Ray Detectable
SOF-WICKLAP PAD
| Applicant | Johnson & Johnson Professionals, Inc., New Brunswick NJ, US |
| Decision | Substantially Equivalent, Jun 28, 1978 |
| Received | May 1, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780718
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.