510(k) K810007 ยท GDB Endoscope, Fiber Optic
PENTAX UPPER G.I. FIBERSCOPE, #FG-34
| Applicant | Pentax Precision Instrument Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 15, 1981 |
| Received | Jan 5, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810007
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.