510(k) K133998 ยท PNO Catheter, Percutaneous, Cutting/Scoring
ANGIOSCULPT PTA SCORING BALLOON WITH HYDROCROSS CAOTING
| Applicant | Angioscore, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Apr 18, 2014 |
| Received | Dec 26, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133998
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.