510(k) K926421 ยท DQY Catheter, Percutaneous
ACS ET HI-FLOW/ENHANCED TORQUE CORONARY GUID CATH
| Applicant | Advanced Cardiovascular Systems, Inc., Temecula CA, US |
| Decision | Substantially Equivalent, Mar 23, 1993 |
| Received | Dec 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926421
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.