510(k) K021469 ยท DQA Oximeter
MINOLTA PULSOX-2
| Applicant | Konica Minolta Sensing, Inc., Denver CO, US |
| Decision | Substantially Equivalent, Feb 12, 2003 |
| Received | May 7, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021469
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.