FDA 510(k) Application Details - K990602

Device Classification Name	More FDA Info for this Device
510(K) Number	K990602
Device Name	RICHTER LIPOPLASTY CANNULAS AND ACCESSORIES
Applicant	TECSA TECHNICAL SERVICES 1205 DE LA VINA SANTA BARBARA, CA 93101 US Other 510(k) Applications for this Company
Contact	CHRISTINE EMANUEL 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	02/24/1999
Decision Date	07/01/1999
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