510(k) K050629 ยท PNO Catheter, Percutaneous, Cutting/Scoring
ANGIOSCULPT SCORING BALLOON CATHETER
| Applicant | Angioscore, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Sep 2, 2005 |
| Received | Mar 11, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050629
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.