510(k) K073360 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
PROPLATE
| Applicant | Bio Protech, Inc., Crofton MD, US |
| Decision | Substantially Equivalent, Dec 19, 2007 |
| Received | Nov 30, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073360
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.