510(k) K073249 ยท DQA Oximeter
SOLARIS NT1 AND NT1A HANDHELD PULSE OXIMETERS WITH SENSOR ACCESSORIES
| Applicant | Solaris Medical Technology, Inc., Great Neck NY, US |
| Decision | Substantially Equivalent, Jul 25, 2008 |
| Received | Nov 19, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073249
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.