510(k) K172221 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
VTRUST Vital Signs Monitor, Model: TD-2300; FORA Vital Signs Monitor, Model: VSM100
| Applicant | Taidoc Technology Corporation, New Taipei City, TW |
| Decision | Substantially Equivalent, Jun 6, 2018 |
| Received | Jul 24, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172221
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.