FDA 510(k) Application Details - K944496

Device Classification Name	Electrode, Electrocardiograph   More FDA Info for this Device
510(K) Number	K944496
Device Name	Electrode, Electrocardiograph
Applicant	MSB LTD. HILLDROP LANE, RAMSBURY MARLBOROUGH, WILTSHIRE SN8 2RB GB Other 510(k) Applications for this Company
Contact	MARTIN BEAUMONT 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	09/13/1994
Decision Date	05/16/1996
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