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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Oximeter
510(k) Number K061896
Device Name MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N; REUSABLE FINGER CLIP SP02 SENSORS, MODEL CST060-2101N
Applicant
MEDIAID INC.
17517 FABRICA WAY #H
CERRITOS,  CA  90703
Applicant Contact MAHESH PATEL
Correspondent
MEDIAID INC.
17517 FABRICA WAY #H
CERRITOS,  CA  90703
Correspondent Contact MAHESH PATEL
Regulation Number870.2700
Classification Product Code
DQA  
Date Received07/03/2006
Decision Date 04/12/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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