510(k) K994344 ยท GXI Probe, Radiofrequency Lesion
NEUROTHERM RF CANNULA
| Applicant | Rocket Medical Plc, Washington, Tyne & Wear, GB |
| Decision | Substantially Equivalent, Mar 21, 2000 |
| Received | Dec 22, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994344
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.