510(k) K972310 ยท DPS Electrocardiograph
NIHON KOHDEN QP-932E ECG EXERCISE TEST OPTION FOR THE NIHON KOHDEN ECG-9320/A CARDIOFAX ELECTROCARDIOGRAPH
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Aug 20, 1997 |
| Received | Jun 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972310
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.