510(k) K093965 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
ULTRAVERSE 014 AND 018 BALLOON DILATATION CATHETERS
| Applicant | C.R. Bard, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Mar 17, 2010 |
| Received | Dec 23, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093965
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.