FDA 510(k) Application Details - K960916

Device Classification Name	Alarm, Blood-Pressure   More FDA Info for this Device
510(K) Number	K960916
Device Name	Alarm, Blood-Pressure
Applicant	3M HEALTH CARE, SARNS 6200 JACKSON RD. ANN ARBOR, MI 48103 US Other 510(k) Applications for this Company
Contact	CHERYL ROSENBERG Other 510(k) Applications for this Contact
Regulation Number	870.1100   More FDA Info for this Regulation Number
Classification Product Code	DSJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/06/1996
Decision Date	06/04/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review