510(k) K101139 ยท KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
PROSTIVA RF THERAPY MODEL 8929 HAND PIECE
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, May 21, 2010 |
| Received | Apr 22, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101139
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.