510(k) K142983 ยท PNO Catheter, Percutaneous, Cutting/Scoring
AngioSculpt PTA Scoring Balloon Catheter with HydroCross Coating
| Applicant | Angioscore, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Mar 4, 2015 |
| Received | Oct 16, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K142983
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.