510(k) K862872 ยท FEI Instrument, Special Lens, For Endoscope
FLEXIBLE VISUALIZATION CATHETER
| Applicant | American Edwards Laboratories, Santa Ana CA, US |
| Decision | Substantially Equivalent, Oct 24, 1986 |
| Received | Jul 30, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862872
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.