510(k) K900451 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
VITALMAX 800 NON-INVASIVE VITAL SIGN MONITOR/PULSE
| Applicant | Pace Tech, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Jul 18, 1990 |
| Received | Jan 30, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900451
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.