510(k) K910852 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
507 NON-INVASIVE VITAL SIGNS MONITOR
| Applicant | Criticare Systems, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jul 30, 1991 |
| Received | Feb 27, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910852
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.