510(k) K070275 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE
| Applicant | Rubicor Medical, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Mar 9, 2007 |
| Received | Jan 29, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070275
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.