510(k) K061931 ยท DQA Oximeter
SOLARIS COMPATIBLE REUSABLE ADULT SPO2 FINGER SENSORS, MODELS S100A-090103 AND 300103, S200A-090101 AND 300101
| Applicant | Solaris Medical Technology, Inc., Las Vegas NV, US |
| Decision | Substantially Equivalent, Jan 31, 2007 |
| Received | Jul 7, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061931
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.