FDA 510(k) Application Details - K991441

Device Classification Name	Monitor, Ultrasonic, Fetal   More FDA Info for this Device
510(K) Number	K991441
Device Name	Monitor, Ultrasonic, Fetal
Applicant	MEDASONICS, INC. 9712 S. ALTAMONT DR. SANDY, UT 84092 US Other 510(k) Applications for this Company
Contact	WILLIAM E MCKAY Other 510(k) Applications for this Contact
Regulation Number	884.2660   More FDA Info for this Regulation Number
Classification Product Code	KNG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/26/1999
Decision Date	12/28/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review