FDA 510(k) Application Details - K953117

Device Classification Name	Digitizer, Image, Radiological   More FDA Info for this Device
510(K) Number	K953117
Device Name	Digitizer, Image, Radiological
Applicant	HOWTEK, INC. 21 PARK AVE. HUDSON, NH 03051 US Other 510(k) Applications for this Company
Contact	M. RUSSELL LEONARD Other 510(k) Applications for this Contact
Regulation Number	892.2030   More FDA Info for this Regulation Number
Classification Product Code	LMA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/03/1995
Decision Date	01/18/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review