510(k) K893867 ยท DQA Oximeter
CARDIAC OUTPUR/SATURATED VENOUS OXYGEN MODULE
| Applicant | Spacelabs, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Sep 13, 1989 |
| Received | May 26, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893867
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.