FDA 510(k) Application Details - K971397

Device Classification Name	Transducer, Ultrasonic, Diagnostic   More FDA Info for this Device
510(K) Number	K971397
Device Name	Transducer, Ultrasonic, Diagnostic
Applicant	QUINTON, INC. 1043 KIEL COURT SUNNYVALE, CA 94089 US Other 510(k) Applications for this Company
Contact	ROY A SMITH Other 510(k) Applications for this Contact
Regulation Number	892.1570   More FDA Info for this Regulation Number
Classification Product Code	ITX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/15/1997
Decision Date	08/25/1997
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