510(k) K040178 ยท DQA Oximeter
PULSEOX 5500 FINGER DEVICE, PULSEOX 7500 WRISTWATCH DEVICE
| Applicant | S.P.O. Medical Equipment, Ltd., Kfar Saba, IL |
| Decision | Substantially Equivalent, Sep 10, 2004 |
| Received | Jan 26, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040178
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.