510(k) K092950 ยท DQA Oximeter
SOLARIS MODELS NT1 AND NT1A HANDHELD PULSE OXIMETERS WITH SENSOR ACCESSORIES
| Applicant | Solaris Medical Technology, Inc., Great Neck NY, US |
| Decision | Substantially Equivalent, Mar 12, 2010 |
| Received | Sep 24, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092950
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.