510(k) K003126 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
BIPOLAR TRIGGER-FLEX PROBE
| Applicant | Ellman Intl., Inc., Hewlett NY, US |
| Decision | Substantially Equivalent, Apr 11, 2001 |
| Received | Oct 5, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003126
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.