S.P.O. Medical Equipment, Ltd.

S.P.O. Medical Equipment, Ltd. holds 1 FDA 510(k) medical device clearance, cleared in 2004.

Top product codes for S.P.O. Medical Equipment, Ltd.

DQA — Cardiovascular1 device

Recent clearances by S.P.O. Medical Equipment, Ltd.

K040178 — PULSEOX 5500 FINGER DEVICE, PULSEOX 7500 WRISTWATCH DEVICECode DQA·2004-09-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.