510(k) K983652 ยท HRX Arthroscope
ABLATOR ELECTRODE
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Mar 23, 1999 |
| Received | Oct 19, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983652
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.