510(k) K925542 ยท DQA Oximeter
OXYSHUTTLE II ,MODIFICATION
| Applicant | Sensor Medics Corp., Yorba Linda CA, US |
| Decision | Substantially Equivalent, Feb 17, 1993 |
| Received | Oct 19, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925542
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 15, 2003 | GE Medical Systems Information Technologies Critikon brand Omni-Stat Finger Sensor - P/N 009084 Terminated |
None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.