FDA 510(k) Application Details - K162881

Device Classification Name	Needle, Assisted Reproduction   More FDA Info for this Device
510(K) Number	K162881
Device Name	Needle, Assisted Reproduction
Applicant	Kitazato Corporation 1-1-8 Shibadaimon, Minato-ku Tokyo 105-0012 JP Other 510(k) Applications for this Company
Contact	Mari YAZAKI Other 510(k) Applications for this Contact
Regulation Number	884.6100   More FDA Info for this Regulation Number
Classification Product Code	MQE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/14/2016
Decision Date	07/11/2017
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