510(k) K061896 ยท DQA Oximeter
MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N; REUSABLE FINGER CLIP SP02 SENSORS, MODEL CST060-2101N
| Applicant | Mediaid, Inc., Cerritos CA, US |
| Decision | Substantially Equivalent, Apr 12, 2007 |
| Received | Jul 3, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061896
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.