510(k) K192318 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Ultraverse 014 and 018 PTA Balloon Dilatation Catheters
| Applicant | Bard Peripheral Vascular, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Oct 3, 2019 |
| Received | Aug 26, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192318
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.