510(k) K101735 ยท PNO Catheter, Percutaneous, Cutting/Scoring
ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2155-XXYY
| Applicant | Angioscore, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Jul 14, 2010 |
| Received | Jun 21, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101735
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.