FDA 510(k) Application Details - K972672

Device Classification Name	Transducer, Ultrasonic, Diagnostic   More FDA Info for this Device
510(K) Number	K972672
Device Name	Transducer, Ultrasonic, Diagnostic
Applicant	BARZELL-WHITMORE MAROON BELLS, INC. 300 NW 82ND AVE., SUITE 402 PLANTATION, FL 33324 US Other 510(k) Applications for this Company
Contact	MARIAN HARDING COCHRAN 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	07/16/1997
Decision Date	07/29/1997
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