510(k) K010732 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
VITALLINK 1200 MOBILE VITAL SIGNS SYSTEMS (VL 1200 SYSTEM)
| Applicant | Telemedic Systems, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Sep 27, 2001 |
| Received | Mar 12, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010732
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.