FDA 510(k) Application Details - K040286

Device Classification Name	Blood Pressure Cuff   More FDA Info for this Device
510(K) Number	K040286
Device Name	Blood Pressure Cuff
Applicant	ETHOX CORP. 251 SENECA ST. BUFFALO, NY 14204 US Other 510(k) Applications for this Company
Contact	EON VERRALL 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	02/06/2004
Decision Date	03/15/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	Y
Expedited Review