FDA 510(k) Application Details - K960218

Device Classification Name	Tube, Aspirating, Flexible, Connecting   More FDA Info for this Device
510(K) Number	K960218
Device Name	Tube, Aspirating, Flexible, Connecting
Applicant	CUSTOM PACK RELIABILITY 4207 VINELAND ROAD, M-1 ORLANDO, FL 32811 US Other 510(k) Applications for this Company
Contact	RICHARD L ELLWOOD Other 510(k) Applications for this Contact
Regulation Number	880.6740   More FDA Info for this Regulation Number
Classification Product Code	BYY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/16/1996
Decision Date	03/28/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review