FDA 510(k) Application Details - K972899

Device Classification Name	Blood Pressure Cuff   More FDA Info for this Device
510(K) Number	K972899
Device Name	Blood Pressure Cuff
Applicant	CYPRESS MEDICAL PRODUCTS, LTD. 1202 SOUTH ROUTE 31 MCHENRY, IL 60050 US Other 510(k) Applications for this Company
Contact	ANTHONY L GIACCIO 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	08/06/1997
Decision Date	07/07/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review