FDA 510(k) Application Details - K951449

Device Classification Name	System, Imaging, Pulsed Echo, Ultrasonic   More FDA Info for this Device
510(K) Number	K951449
Device Name	System, Imaging, Pulsed Echo, Ultrasonic
Applicant	KOVEN TECHNOLOGY, INC. 300 BROOKES DR. SUITE 105 ST. LOUIS, MO 63042 US Other 510(k) Applications for this Company
Contact	PAUL G KOVEN Other 510(k) Applications for this Contact
Regulation Number	892.1560   More FDA Info for this Regulation Number
Classification Product Code	IYO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/29/1995
Decision Date	05/20/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review