FDA 510(k) Application Details - K201305

Device Classification Name	Apparatus, Autotransfusion   More FDA Info for this Device
510(K) Number	K201305
Device Name	Apparatus, Autotransfusion
Applicant	Atrium Medical Corporation 40 Continental Blvd. Merrimack, NH 03054 US Other 510(k) Applications for this Company
Contact	Robin Mulvey 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	05/15/2020
Decision Date	09/03/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review