FDA 510(k) Application Details - K021171

Device Classification Name	Electrocardiograph   More FDA Info for this Device
510(K) Number	K021171
Device Name	Electrocardiograph
Applicant	MEDICAL POSITIONING, INC. 21911 ERIE LN. LAKE FOREST, CA 92630 US Other 510(k) Applications for this Company
Contact	CAROL PATTERSON Other 510(k) Applications for this Contact
Regulation Number	870.2340   More FDA Info for this Regulation Number
Classification Product Code	DPS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/12/2002
Decision Date	05/08/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review