510(k) K052693 ยท DQA Oximeter
PM-50 PULSE OXIMETER
| Applicant | Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Great Neck NY, US |
| Decision | Substantially Equivalent, Mar 30, 2006 |
| Received | Sep 28, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052693
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.