510(k) K092652 ยท DQA Oximeter
FINGERTIP PULSE OXIMETER, MODEL MD300CA ND300CA
| Applicant | Beijing Choice Electronic Technololgy Co., Ltd., Beijing, CN |
| Decision | Substantially Equivalent, Jan 8, 2010 |
| Received | Aug 28, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092652
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.