510(k) K910629 ยท DQA Oximeter
AP-860PA NIBP MODULE
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, May 14, 1991 |
| Received | Feb 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910629
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.