510(k) K030890 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
SWITCHBLADE
| Applicant | Snowden Pencer, Inc., Tucker GA, US |
| Decision | Substantially Equivalent, Apr 4, 2003 |
| Received | Mar 21, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030890
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.