510(k) K941239 ยท GWG Endoscope, Neurological
AESCULAP NEUROENDOSCOPE
| Applicant | Aesculap, Inc., South San Francisco CA, US |
| Decision | Substantially Equivalent, Jul 11, 1994 |
| Received | Mar 15, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941239
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.