510(k) K901612 ยท DQA Oximeter
VITALMAX 2000 ECG MONITOR W/NON-INVASIVE BLOOD-PRE
| Applicant | Pace Tech, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Apr 30, 1990 |
| Received | Apr 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901612
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.