510(k) K952524 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
AESCULAP BIOPOLAR COAGULATOR
| Applicant | Aesculap, Inc., South San Francisco CA, US |
| Decision | Substantially Equivalent, Jun 29, 1995 |
| Received | Jun 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952524
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 11, 2013 | Aesculap, Inc. Aesculap GNI161 Bipolar Foot Control
Product Usage:
The Aesculap Bipolar Coagulator is intended for use in surgery to generate electrical power for bipolar instruments. Bipolar coagulators are used i Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.