510(k) K952205 ยท DQY Catheter, Percutaneous
ACS POWERBASE GUILDING CATHETER
| Applicant | Advanced Cardiovascular Systems, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Aug 4, 1995 |
| Received | May 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952205
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.