510(k) K974697 ยท DQH Cardiograph, Apex (Vibrocardiograph)
REUSABLE FINGER SENSOR 3444
| Applicant | Bci Intl., Inc., Waukesha WI, US |
| Decision | Substantially Equivalent, Mar 11, 1998 |
| Received | Dec 16, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974697
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.