510(k) K791703 ยท GDI Dissector, Surgical, General & Plastic Surgery
TEW BYPASS INSTRUMENTS & DISSECTING KIT
| Applicant | Edward Weck, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 4, 1979 |
| Received | Aug 28, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791703
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.