FDA 510(k) Application Details - K053000

Device Classification Name	Apparatus, Autotransfusion   More FDA Info for this Device
510(K) Number	K053000
Device Name	Apparatus, Autotransfusion
Applicant	HAEMONETICS CORP. 400 WOOD ROAD BRAINTREE, MA 02184-9114 US Other 510(k) Applications for this Company
Contact	GABRIEL J MURACA Other 510(k) Applications for this Contact
Regulation Number	868.5830   More FDA Info for this Regulation Number
Classification Product Code	CAC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/25/2005
Decision Date	11/21/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review