510(k) K203461 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Aesculap Caiman 12 Seal and Cut Technology System
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Dec 18, 2020 |
| Received | Nov 24, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K203461
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.