510(k) K101694 ยท DQA Oximeter
HANDHELD PULSE OXIMETER MODEL M800
| Applicant | Guangdong Biolight Meditech Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Sep 8, 2010 |
| Received | Jun 16, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101694
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.