FDA 510(k) Application Details - K961453

Device Classification Name	Cassette, Radiographic Film   More FDA Info for this Device
510(K) Number	K961453
Device Name	Cassette, Radiographic Film
Applicant	EASTMAN KODAK COMPANY 1669 LAKE AVE. ROCHESTER, NY 14652 US Other 510(k) Applications for this Company
Contact	HENRY J PINK Other 510(k) Applications for this Contact
Regulation Number	892.1850   More FDA Info for this Regulation Number
Classification Product Code	IXA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/16/1996
Decision Date	07/25/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review