510(k) K893221 ยท DQA Oximeter
MODEL 8500 HAND HELD PULSE OXIMETER
| Applicant | Nonin Medical, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 28, 1990 |
| Received | Apr 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893221
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 29, 2016 | Nonin Medical, Inc 8500M Handheld Pulse Oximeter Terminated |
DQA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.