510(k) K112182 ยท PNO Catheter, Percutaneous, Cutting/Scoring
ANGIOSCULPT PTA SCORING BALLOON CATHETER
| Applicant | Angioscore, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Aug 26, 2011 |
| Received | Jul 28, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112182
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.