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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 K110893
Device Name VTRUST FINGER TYPE PULSE OXIMETER
Applicant
TaiDoc Technology Corporation
3F, 5F, NO 127 WUGONG 2ND RD
WUGU TOWNSHIP
TAIPEI COUNTY,  TW 24888
Applicant Contact TELING HSU
Correspondent
TaiDoc Technology Corporation
3F, 5F, NO 127 WUGONG 2ND RD
WUGU TOWNSHIP
TAIPEI COUNTY,  TW 24888
Correspondent Contact TELING HSU
Regulation Number870.2700
Classification Product Code
DQA  
Date Received03/30/2011
Decision Date 11/22/2011
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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