FDA 510(k) Application Details - K161547

Device Classification Name	Catheter, Assisted Reproduction   More FDA Info for this Device
510(K) Number	K161547
Device Name	Catheter, Assisted Reproduction
Applicant	ORIGIO A/S KNARDRUPVEJ 2 MAALOEV 2760 DK Other 510(k) Applications for this Company
Contact	TOVE KJAER Other 510(k) Applications for this Contact
Regulation Number	884.6110   More FDA Info for this Regulation Number
Classification Product Code	MQF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/03/2016
Decision Date	03/09/2017
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