510(k) K101259 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
V-TRUST TD-8002 MULTI-PARAMETER SPOT-CHECK MONITOR MODEL TD-8002
| Applicant | Taidoc Technology Corporation, New Taipei City, TW |
| Decision | Substantially Equivalent, Jun 17, 2010 |
| Received | May 4, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101259
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.