FDA 510(k) Application Details - K103009

Device Classification Name	Reminder, Medication   More FDA Info for this Device
510(K) Number	K103009
Device Name	Reminder, Medication
Applicant	SENTICARE, INC. 401 9TH STREET NW SUITE 900 WASHINGTON, DC 20004 US Other 510(k) Applications for this Company
Contact	SETH A MAILHOT 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	10/12/2010
Decision Date	01/28/2011
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