510(k) K980299 ยท DQA Oximeter
APEX OXIMETER
| Applicant | Marquette Medical Systems, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Apr 24, 1998 |
| Received | Jan 27, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980299
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 13, 2010 | General Electric Medical Systems Information Technology GE ApexPro Oximeter systems (ApexPro CH or ApexPro FH with ApexPro Telemetry version 3.9 software) Terminated |
DQA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.