510(k) K962321 ยท HRX Arthroscope
ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970
| Applicant | Arthrocare Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jul 19, 1996 |
| Received | Jun 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962321
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.