510(k) K881307 ยท DQA Oximeter
OLV 1100; OLV 1200 PULSE OXIMETERS
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Nov 4, 1988 |
| Received | Mar 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881307
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.