510(k) K053419 ยท DQA Oximeter
KONICA MINOLTA PULSOX-300, 300I
| Applicant | Konica Minolta Sensing, Inc., Denver CO, US |
| Decision | Substantially Equivalent, May 11, 2006 |
| Received | Dec 8, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053419
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.