510(k) K873795 ยท FEI Instrument, Special Lens, For Endoscope
M-LENS (THIRTY DEGREE ENDOSCOPE)
| Applicant | Opto Vision, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Jan 14, 1988 |
| Received | Sep 17, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873795
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.