FDA 510(k) Application Details - K032802

Device Classification Name	More FDA Info for this Device
510(K) Number	K032802
Device Name	HK LIPOSUCTION ASPIRATOR, MODEL AP-III & AP230-III
Applicant	HK SURGICAL, INC. 2620A TEMPLE HEIGHTS DR. OCEANSIDE, CA 92675 US Other 510(k) Applications for this Company
Contact	SALLY M BOWDON Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QPB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/09/2003
Decision Date	11/19/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review