510(k) K980636 ยท FFS Image, Illumination, Fiberoptic, For Endoscope
FIBER OPTIC ENDOILLUMINATION PROBE
| Applicant | Dutch Ophthalmic USA, Inc., Kingston NH, US |
| Decision | Substantially Equivalent, May 20, 1998 |
| Received | Feb 19, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980636
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.