510(k) K905274 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
VITALMAX 2100/2200
| Applicant | Pace Tech, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Jul 17, 1991 |
| Received | Nov 15, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905274
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.