FDA 510(k) Application Details - K982427

Device Classification Name	More FDA Info for this Device
510(K) Number	K982427
Device Name	TREX TILT C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM, TREX TILT-C
Applicant	TREX MEDICAL CORP. 2000 SOUTH 25TH AVE. BROADVIEW, IL 60153 US Other 510(k) Applications for this Company
Contact	WILLIAM T COUSINS Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OWB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/13/1998
Decision Date	09/23/1998
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