FDA 510(k) Application Details - K160502

Device Classification Name	System, Multipurpose For In Vitro Coagulation Studies   More FDA Info for this Device
510(K) Number	K160502
Device Name	System, Multipurpose For In Vitro Coagulation Studies
Applicant	Haemonetics Corporation 400 Wood Road Braintree, MA 02184 US Other 510(k) Applications for this Company
Contact	Paige Sweeney 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	02/23/2016
Decision Date	04/19/2017
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