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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 STREET NW
SUITE 900
WASHINGTON,  DC  20004
Applicant Contact SETH A MAILHOT
Correspondent
SENTICARE, INC.
401 9TH STREET 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
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