510(k) K181323 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Atlas Gold PTA Dilatation Catheter
| Applicant | C.R. Bard, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Aug 3, 2018 |
| Received | May 18, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181323
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.