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FDA 510(k) Applications Submitted by MEDIAID INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K071610
06/13/2007
MEDIAID PULSE OXIMETER M30 AND M34
MEDIAID INC.
K071642
06/18/2007
MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER
MEDIAID INC.
K041964
07/21/2004
MEDIAID REUSABLE FINGER CLIP SPO2 SENSORS AND DISPOSABLE NON-ADHESIVE SENSORS AND ADHESIVE SPO2 SENSORS
MEDIAID INC.
K061896
07/03/2006
MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N; REUSABLE FINGER CLIP SP02 SENSORS, MODEL CST060-2101N
MEDIAID INC.
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