510(k) K100303 ยท PNO Catheter, Percutaneous, Cutting/Scoring
ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2076-XXYY, 2092-XXYY, 2105-XXYY
| Applicant | Angioscore, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Mar 22, 2010 |
| Received | Feb 3, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100303
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.