510(k) K832006 ยท FDT Duodenoscope And Accessories, Flexible/Rigid
PENTAX FD-34A DUODENOFIBERSCOPE
| Applicant | Pentax Precision Instrument Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 1, 1983 |
| Received | Jun 23, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832006
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.