510(k) K082846 ยท DQA Oximeter
APK SPO2 PULSE OXIMETER SENSOR
| Applicant | APK Technology Co., Ltd., No. 2 Road(S); Shanghai, CN |
| Decision | Substantially Equivalent, Apr 3, 2009 |
| Received | Sep 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082846
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.