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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 K071610
Device Name MEDIAID PULSE OXIMETER M30 AND M34
Applicant
MEDIAID INC.
17517 FABRICA WAY, SUITE H
CERRITOS,  CA  90703
Applicant Contact JAYESH PATEL
Correspondent
MEDIAID INC.
17517 FABRICA WAY, SUITE H
CERRITOS,  CA  90703
Correspondent Contact JAYESH PATEL
Regulation Number870.2700
Classification Product Code
DQA  
Date Received06/13/2007
Decision Date 11/05/2007
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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