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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 K071642
Device Name MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER
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  
Subsequent Product Code
DXN  
Date Received06/18/2007
Decision Date 05/02/2008
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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