510(k) K882273 ยท DQA Oximeter
HORIZON 2000 PULSE OXIMETRY AND MODULE
| Applicant | Mennen Medical, Inc., Clarence NY, US |
| Decision | Substantially Equivalent, Aug 25, 1988 |
| Received | May 31, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882273
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.