510(k) K110695 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
BIPOLAR HF DEVICE
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jun 28, 2011 |
| Received | Mar 14, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110695
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.