510(k) K960400 ยท FBM Cannula And Trocar, Suprapubic, Non-Disposable
DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS)
| Applicant | Snowden-Pencer, Tucker GA, US |
| Decision | Substantially Equivalent, Mar 12, 1996 |
| Received | Jan 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960400
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.