510(k) K000252 ยท MPA Endoilluminator
INSIGHT 4000 ENDOSCOPE
| Applicant | Insight Instruments Mfg., Inc., Sanford FL, US |
| Decision | Substantially Equivalent, Oct 17, 2000 |
| Received | Jan 27, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000252
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.