510(k) K943022 ยท DQX Wire, Guide, Catheter
CARDIOMETRICS FLOWIRE DOPPLER GUIDE WIRE
| Applicant | Cardio Metrics, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Sep 19, 1994 |
| Received | Jun 24, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943022
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.