FDA 510(k) Application Details - K990913

Device Classification Name	Needle, Assisted Reproduction   More FDA Info for this Device
510(K) Number	K990913
Device Name	Needle, Assisted Reproduction
Applicant	LABORATOIRES PRODIMED 23 WELISEWITZ RD. RINGOES, NJ 08551 US Other 510(k) Applications for this Company
Contact	RANDOLPH L COOKE 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	03/18/1999
Decision Date	06/08/1999
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