FDA 510(k) Application Details - K992308

Device Classification Name	Needle, Assisted Reproduction   More FDA Info for this Device
510(K) Number	K992308
Device Name	Needle, Assisted Reproduction
Applicant	LIFETEK MEDICAL, INC. P.O. BOX 560 STILLWATER, MN 55082 US Other 510(k) Applications for this Company
Contact	ELAINE DUNCAN 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	07/09/1999
Decision Date	09/13/1999
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