FDA 510(k) Application Details - K954183

Device Classification Name	Contraception Calculator   More FDA Info for this Device
510(K) Number	K954183
Device Name	Contraception Calculator
Applicant	HECTOR VIDES 3652 N. RICHMOND CHICAGO, IL 60618 US Other 510(k) Applications for this Company
Contact	HECTOR VIDES Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MPT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/06/1995
Decision Date	02/29/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review