510(k) K023358 ยท FGB Ureteroscope And Accessories, Flexible/Rigid
USA SERIES DUR 8 ELITE, USA SERIES DUR 8, MODELS DUR 8E, DUR 8
| Applicant | Acmi Corporation, Southborough MA, US |
| Decision | Substantially Equivalent, Jan 3, 2003 |
| Received | Oct 7, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023358
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.