510(k) K884536 ยท DQA Oximeter
AL-800PA PULSE OXIMETER MODULE
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Feb 6, 1989 |
| Received | Oct 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884536
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.