510(k) K932203 ยท DQA Oximeter
VITALMAX 530
| Applicant | Pace Tech Medical Monitors, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Jul 19, 1994 |
| Received | May 6, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932203
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.