510(k) K120537 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
AQUAMANTYS3 9.5 XL BIPOLAR SEALER
| Applicant | Medtronic, Inc., Portsmouth NH, US |
| Decision | Substantially Equivalent, May 10, 2012 |
| Received | Feb 22, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120537
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.