510(k) K014149 ยท GWG Endoscope, Neurological
PAEDISCOPE, MODEL # P010A AND PF011A
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Mar 18, 2002 |
| Received | Dec 18, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014149
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.