FDA 510(k) Applications Submitted by S.P.O. MEDICAL EQUIPMENT, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K040178 | 01/26/2004 | PULSEOX 5500 FINGER DEVICE, PULSEOX 7500 WRISTWATCH DEVICE | S.P.O. MEDICAL EQUIPMENT, LTD. |
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