FDA 510(k) Application Details - K152932

Device Classification Name	Media, Reproductive   More FDA Info for this Device
510(K) Number	K152932
Device Name	Media, Reproductive
Applicant	ORIGIO A/S KNARDRUPVEJ 2 MALOV 2760 DK Other 510(k) Applications for this Company
Contact	TOVE KJAER 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	10/05/2015
Decision Date	02/29/2016
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