510(k) K895987 ยท DQA Oximeter
KELLER PULSE OXIMETER - KMS 850
| Applicant | Keller Medical Specialties Products, Inc., Antioch IL, US |
| Decision | Substantially Equivalent, Feb 22, 1990 |
| Received | Oct 12, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895987
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.