510(k) K884262 ยท DQX Wire, Guide, Catheter
ACS(R) HI-TORQUE GOLD(TM) GUIDE WIRE
| Applicant | Advanced Cardiovascular Systems, Inc., Temecula CA, US |
| Decision | Substantially Equivalent, Dec 21, 1988 |
| Received | Oct 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884262
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.