510(k) K072217 ยท DPS Electrocardiograph
ECG-1250A SERIES CARDIOFAX S AND ECG-1350A SERIES CARDIOFAX M
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, Aug 30, 2007 |
| Received | Aug 9, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072217
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.