FDA 510(k) Application Details - K060089

Device Classification Name	More FDA Info for this Device
510(K) Number	K060089
Device Name	TULIP DISPOSABLE CANNULAS
Applicant	CELL BIO-SYSTEMS, INC. 1205 DE LA VINA STREET 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	01/12/2006
Decision Date	04/27/2006
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