510(k) K922302 ยท DQX Wire, Guide, Catheter
JAGWIRE(TM) RECANALIZATION GUIDEWIRE
| Applicant | Boston Scientific Corp, San Jose CA, US |
| Decision | Substantially Equivalent, Jul 24, 1992 |
| Received | May 15, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922302
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.