FDA 510(k) Application Details - K133568

Device Classification Name	Media, Reproductive   More FDA Info for this Device
510(K) Number	K133568
Device Name	Media, Reproductive
Applicant	VITROLIFE, INC. 3601 SOUTH INCA ST. ENGLEWOOD, CO 80110 US Other 510(k) Applications for this Company
Contact	MARK LARMAN Other 510(k) Applications for this Contact
Regulation Number	884.6180   More FDA Info for this Regulation Number
Classification Product Code	MQL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/20/2013
Decision Date	07/16/2014
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