FDA 510(k) Application Details - K070232

Device Classification Name	Cable, Transducer And Electrode, Patient, (Including Connector)   More FDA Info for this Device
510(K) Number	K070232
Device Name	Cable, Transducer And Electrode, Patient, (Including Connector)
Applicant	AMERICAN I.V. PRODUCTS, INC. 7485 SHIPLEY AVE. HARMANS, MD 21077 US Other 510(k) Applications for this Company
Contact	JOHN TAYLOR Other 510(k) Applications for this Contact
Regulation Number	870.2900   More FDA Info for this Regulation Number
Classification Product Code	DSA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/24/2007
Decision Date	03/27/2007
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	N
Expedited Review