510(k) K964594 ยท KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
VAPORTRODE VAPORIZATION ELECTRODE -GROOVED/FLUTED/SPIKED(GVE-B,GVE-F,GVE-S) & VAPORTOMME VAPORIZATION LOOP (GVE-LG)
| Applicant | Circon Corp., Stamford CT, US |
| Decision | Substantially Equivalent, Aug 15, 1997 |
| Received | Nov 15, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964594
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.