FDA 510(k) Application Details - K060298

Device Classification Name	Reminder, Medication   More FDA Info for this Device
510(K) Number	K060298
Device Name	Reminder, Medication
Applicant	VOCEL 1425 K STREET, N.W. SUITE 1100 WASHINGTON, DC 20005 US Other 510(k) Applications for this Company
Contact	KEITH A BARRITT Other 510(k) Applications for this Contact
Regulation Number	890.5050   More FDA Info for this Regulation Number
Classification Product Code	NXQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/06/2006
Decision Date	03/29/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review