510(k) K822393 ยท DQY Catheter, Percutaneous
INTRAOPERATIVE BALLOON DILATION CATH.
| Applicant | Advanced Cardiovascular Systems, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 1, 1982 |
| Received | Aug 9, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822393
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.