FDA 510(k) Application Details - K993934

Device Classification Name	Electrode, Electrocardiograph   More FDA Info for this Device
510(K) Number	K993934
Device Name	Electrode, Electrocardiograph
Applicant	VQ CORP. 3130 HIGHLAND AVE. THIRD FLOOR CINCINNATI, OH 45219-2374 US Other 510(k) Applications for this Company
Contact	MICHAEL A PRICE Other 510(k) Applications for this Contact
Regulation Number	870.2360   More FDA Info for this Regulation Number
Classification Product Code	DRX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/18/1999
Decision Date	08/15/2000
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