510(k) K822597 ยท DQX Wire, Guide, Catheter
GUIDE WIRE
| Applicant | Vertex Medical Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 21, 1982 |
| Received | Aug 27, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822597
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.