510(k) K991989 ยท GWG Endoscope, Neurological
MITAKA POINT SETTER
| Applicant | Mitaka USA, Inc., Park City UT, US |
| Decision | Substantially Equivalent, Aug 27, 1999 |
| Received | Jun 14, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991989
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.