510(k) K122685 ยท PNO Catheter, Percutaneous, Cutting/Scoring
ANGIOSCULPT PTA SCORING BALLOON CATHETER
| Applicant | Angioscore, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Jan 11, 2013 |
| Received | Aug 31, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122685
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.