FDA 510(k) Application Details - K022922

Device Classification Name	Test, Time, Prothrombin   More FDA Info for this Device
510(K) Number	K022922
Device Name	Test, Time, Prothrombin
Applicant	LIFESCAN, INC. 1000 GIBRALTAR DR. MILPITAS, CA 95035-6312 US Other 510(k) Applications for this Company
Contact	JOHN E HUGHES Other 510(k) Applications for this Contact
Regulation Number	864.7750   More FDA Info for this Regulation Number
Classification Product Code	GJS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/04/2002
Decision Date	09/30/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	HE - Hematology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review