510(k) K900272 ยท DPS Electrocardiograph
NKA MODELS AB-601G AND AB-621G
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 31, 1990 |
| Received | Jan 10, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900272
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.