510(k) K151858 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Caiman Seal and Cut Technology
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jul 21, 2015 |
| Received | Jul 8, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151858
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 16, 2017 | Aesculap Implant Systems LLC GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.