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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Reminder, Medication
510(k) Number K103009
Device Name SENTICARE PILLSTATION
Applicant
Senticare, Inc.
401 9th St. NW
Suite 900
Washington,  DC  20004
Applicant Contact SETH A MAILHOT
Correspondent
Senticare, Inc.
401 9th St. NW
Suite 900
Washington,  DC  20004
Correspondent Contact SETH A MAILHOT
Regulation Number890.5050
Classification Product Code
NXQ  
Date Received10/12/2010
Decision Date 01/28/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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