510(k) K110767 ยท PNO Catheter, Percutaneous, Cutting/Scoring
ANGIOSCULPT PTA SCORING BALLOON CATHETER
| Applicant | Angioscore, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Apr 15, 2011 |
| Received | Mar 18, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110767
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.