FDA 510(k) Application Details - K954294

Device Classification Name	Grid, Radiographic   More FDA Info for this Device
510(K) Number	K954294
Device Name	Grid, Radiographic
Applicant	THERMOTREX CORP. 36 APPLE RIDGE RD. DANBURY, CT 06810 US Other 510(k) Applications for this Company
Contact	JEFFREY MOELLER Other 510(k) Applications for this Contact
Regulation Number	892.1910   More FDA Info for this Regulation Number
Classification Product Code	IXJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/14/1995
Decision Date	02/02/1996
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