FDA 510(k) Application Details - K961424

Device Classification Name	Transducer, Pressure, Intrauterine   More FDA Info for this Device
510(K) Number	K961424
Device Name	Transducer, Pressure, Intrauterine
Applicant	UTAH MEDICAL PRODUCTS, INC. 7043 SOUTH 300 WEST MIDVALE, UT 84047-1048 US Other 510(k) Applications for this Company
Contact	KEVIN L CORNWELL Other 510(k) Applications for this Contact
Regulation Number	884.2700   More FDA Info for this Regulation Number
Classification Product Code	HFN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/12/1996
Decision Date	07/10/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review