FDA 510(k) Application Details - K002954

Device Classification Name	Blood Pressure Cuff   More FDA Info for this Device
510(K) Number	K002954
Device Name	Blood Pressure Cuff
Applicant	RUDOLF RIESTER GMBH & CO. KG BRUCKSTRASSE 31 P.O. BOX 35 JUNGINGEN D-72417 DE Other 510(k) Applications for this Company
Contact	PATRICIA RIESTER-FREUDENMANN Other 510(k) Applications for this Contact
Regulation Number	870.1120   More FDA Info for this Regulation Number
Classification Product Code	DXQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/22/2000
Decision Date	12/21/2000
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