FDA 510(k) Application Details - K112644

Device Classification Name	Labware, Assisted Reproduction   More FDA Info for this Device
510(K) Number	K112644
Device Name	Labware, Assisted Reproduction
Applicant	LOTUS BIO LTD 461 MAIN STREET SUITE 217 PAWTUCKET, RI 02860 US Other 510(k) Applications for this Company
Contact	LORI KAHLER Other 510(k) Applications for this Contact
Regulation Number	884.6160   More FDA Info for this Regulation Number
Classification Product Code	MQK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/12/2011
Decision Date	12/19/2012
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