510(k) K092761 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
PROPLATE, MODELS 9641C, 9641F, P9641C, P9641F, 9642C, 9642F AND P9642C
| Applicant | Bio Protech, Inc., Dallas TX, US |
| Decision | Substantially Equivalent, Nov 24, 2009 |
| Received | Sep 9, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092761
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.