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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