510(k) K010013 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
LIGASURE LAPAROSCOPIC SEALER DIVIDER MODEL LS1100
| Applicant | Valleylab, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Mar 26, 2001 |
| Received | Jan 2, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010013
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 19, 2006 | Covidien LP LigaSure Atlas Laparoscopic Vessel Sealer/Divider Terminated |
GEI | None listed |
| Apr 19, 2006 | Covidien LP LigaSure Atlas 20 cm Open Procedure Vessel Sealer/Divider Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.