FDA 510(k) Application Details - K012042

Device Classification Name	More FDA Info for this Device
510(K) Number	K012042
Device Name	KINETIC CANNULA
Applicant	RELIANCE MEDICAL CORP. 730 INDEPENDENT AVE. GRAND JUNCTION, CO 81505 US Other 510(k) Applications for this Company
Contact	ROBERT W NICKS 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	06/29/2001
Decision Date	09/20/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review