FDA 510(k) Application Details - K974432

Device Classification Name	System, Imaging, Pulsed Echo, Ultrasonic   More FDA Info for this Device
510(K) Number	K974432
Device Name	System, Imaging, Pulsed Echo, Ultrasonic
Applicant	ULTRAGUIDE LTD. 377 ROUTE 17 SOUTH HASBROUCK HEIGHTS, NJ 07601 US Other 510(k) Applications for this Company
Contact	GEORGE H MYERS 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	11/24/1997
Decision Date	02/09/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review