510(k) K955598 ยท GWG Endoscope, Neurological
CLARUS SPINEPEN MODEL 2126
| Applicant | Clarus Medical Systems, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 6, 1996 |
| Received | Dec 8, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955598
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.