510(k) K833924 ยท FDS Gastroscope And Accessories, Flexible/Rigid
TWO CHANNEL GASTROFIBERSCOPE FG-36T
| Applicant | Pentax Precision Instrument Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 4, 1984 |
| Received | Nov 14, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833924
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.