510(k) K101012 ยท DQA Oximeter
V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201
| Applicant | Taidoc Technology Corporation, Taipei County, TW |
| Decision | Substantially Equivalent, Dec 15, 2010 |
| Received | Apr 12, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101012
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.