510(k) K981916 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
LIGASURE VESSEL SEALING SYSTEM
| Applicant | Valleylab, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Aug 28, 1998 |
| Received | Jun 1, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981916
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.