510(k) K982331 ยท DQA Oximeter
KELLER PULSE OXIMETER, MODEL 850+
| Applicant | Keller Medical Specialties Products, Inc., Antioch IL, US |
| Decision | Substantially Equivalent, Sep 11, 1998 |
| Received | Jul 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982331
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.