510(k) K091966 ยท PNO Catheter, Percutaneous, Cutting/Scoring
ANGIOSCULPT PTA SCORING BALLOON CATHETER, MODELS 2076-6040, 2092-6040, 2105-6040
| Applicant | Angioscore, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Jul 30, 2009 |
| Received | Jul 1, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091966
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.