510(k) K052511 ยท DPS Electrocardiograph
CARDIOFAX CE, MODEL ECG-1500 A
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, May 24, 2006 |
| Received | Sep 14, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052511
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.