FDA 510(k) Application Details - K970090

Device Classification Name	Cassette, Radiographic Film   More FDA Info for this Device
510(K) Number	K970090
Device Name	Cassette, Radiographic Film
Applicant	SOLO-SLED, LLC. 2413 VANCE AVE. P.O.BOX 3718 CHATTANOOGA, TN 37404 US Other 510(k) Applications for this Company
Contact	PATRICIA A RODDY 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	01/10/1997
Decision Date	04/21/1997
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