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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 K060298
Device Name PILL PHONE
Applicant
Vocel
1425 K St., NW, Suite 1100
Washington,  DC  20005
Applicant Contact KEITH A BARRITT
Correspondent
Vocel
1425 K St., NW, Suite 1100
Washington,  DC  20005
Correspondent Contact KEITH A BARRITT
Regulation Number890.5050
Classification Product Code
NXQ  
Date Received02/06/2006
Decision Date 03/29/2006
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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