510(k) K101577 ยท DQA Oximeter
MODIFICATION TO:FINGERTIP PULSE OXIMETER, MODEL MD300C SERIES
| Applicant | Beijing Choice Electronic Technololgy Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Dec 2, 2010 |
| Received | Jun 7, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101577
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.