510(k) K101602 ยท MLD Monitor, St Segment With Alarm
VITAL SIGNS MONITOR
| Applicant | Criticare Systems, Inc., Waukesha WI, US |
| Decision | Substantially Equivalent, Sep 1, 2010 |
| Received | Jun 8, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101602
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.