FDA 510(k) Application Details - K041689

Device Classification Name	Blood Pressure Cuff   More FDA Info for this Device
510(K) Number	K041689
Device Name	Blood Pressure Cuff
Applicant	D. E. HOKANSON, INC. 12840 N.E. 21ST PL. BELLEVUE, WA 98005-1910 US Other 510(k) Applications for this Company
Contact	D. EUGENE HOKANSON 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	06/22/2004
Decision Date	08/06/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review