510(k) K071482 ยท GXD Generator, Lesion, Radiofrequency
STRYKER RF MULTI-LESION GENERATOR, MODEL 0406-900-000
| Applicant | Synergetics, Inc., O' Fallon MO, US |
| Decision | Substantially Equivalent, Dec 20, 2007 |
| Received | May 30, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071482
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 16, 2016 | Stryker Instruments Div. of Stryker Corporation RF MultiGen, 0406-900-000; Refurb RF MultiGen, 0406-900-000U Terminated |
GXD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.