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S.P.O. Medical Equipment, Ltd.

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K040178 PULSEOX 5500 FINGER DEVICE, PULSEOX 7500 WRISTWATCH DEVICEDQA2004-09-10 View
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