FDA 510(k) Application Details - K022021

Device Classification Name	Activated Partial Thromboplastin   More FDA Info for this Device
510(K) Number	K022021
Device Name	Activated Partial Thromboplastin
Applicant	VITAL SCIENTIFIC N.V. ONE GATEWAY CENTER SUITE 411 NEWTON, MA 02458 US Other 510(k) Applications for this Company
Contact	ISRAEL M STEIN Other 510(k) Applications for this Contact
Regulation Number	864.7925   More FDA Info for this Regulation Number
Classification Product Code	GFO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/20/2002
Decision Date	11/01/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	HE - Hematology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review