510(k) K982133 ยท HRX Arthroscope
OLYMPUS ENDOSCOPIC SYSTEM LUMBAR HERNIA DISCECTOMY AND ITS ANCILLARY EQUIPMENT
| Applicant | The Olympus Optical Co., North Attleboro MA, US |
| Decision | Substantially Equivalent, Oct 22, 1998 |
| Received | Jun 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982133
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.