FDA 510(k) Application Details - K971022

Device Classification Name	Apparatus, Suction, Operating-Room, Wall Vacuum Powered   More FDA Info for this Device
510(K) Number	K971022
Device Name	Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Applicant	CHASE MEDICAL, INC. 1876 FIRMAN DR. RICHARDSON, TX 75081 US Other 510(k) Applications for this Company
Contact	BERT DAVIS Other 510(k) Applications for this Contact
Regulation Number	880.6740   More FDA Info for this Regulation Number
Classification Product Code	GCX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/20/1997
Decision Date	04/17/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review