510(k) K001020 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
8100 VITAL SIGNS MONITOR
| Applicant | Criticare Systems, Inc., Waukesha WI, US |
| Decision | Substantially Equivalent, Apr 28, 2000 |
| Received | Mar 30, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001020
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.