FDA 510(k) Application Details - K022306

Device Classification Name	Accessories, Catheter   More FDA Info for this Device
510(K) Number	K022306
Device Name	Accessories, Catheter
Applicant	AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. 5871 LONE PINE PLACE PASO ROBLES, CA 93446 US Other 510(k) Applications for this Company
Contact	CATHERINE RIPLE Other 510(k) Applications for this Contact
Regulation Number	878.4200   More FDA Info for this Regulation Number
Classification Product Code	KGZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/16/2002
Decision Date	10/10/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review