510(k) K072581 ยท DQA Oximeter
PM-60 PULSE OXIMETER
| Applicant | Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Great Neck NY, US |
| Decision | Substantially Equivalent, Jan 8, 2008 |
| Received | Sep 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072581
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.