FDA 510(k) Application Details - K083842

Device Classification Name	System, Multipurpose For In Vitro Coagulation Studies   More FDA Info for this Device
510(K) Number	K083842
Device Name	System, Multipurpose For In Vitro Coagulation Studies
Applicant	PENTAPHARM GMBH STAHLGRUBERRING 12 MUNICH D-81829 DE Other 510(k) Applications for this Company
Contact	VOLKER JOACHIM FRIEMERT Other 510(k) Applications for this Contact
Regulation Number	864.5425   More FDA Info for this Regulation Number
Classification Product Code	JPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/24/2008
Decision Date	03/23/2010
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