FDA 510(k) Application Details - K024170

Device Classification Name	Lancet, Blood   More FDA Info for this Device
510(K) Number	K024170
Device Name	Lancet, Blood
Applicant	PELIKAN TECHNOLOGIES, INC 1072 EAST MEADOW CIRCLE PALO ALTO, CA 94303 US Other 510(k) Applications for this Company
Contact	JACK GREEN Other 510(k) Applications for this Contact
Regulation Number	878.4800   More FDA Info for this Regulation Number
Classification Product Code	FMK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/18/2002
Decision Date	04/14/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review