FDA 510(k) Application Details - K003142

Device Classification Name	Micromanipulators And Microinjectors, Assisted Reproduction   More FDA Info for this Device
510(K) Number	K003142
Device Name	Micromanipulators And Microinjectors, Assisted Reproduction
Applicant	RESEARCH INSTRUMENTS LTD. KERNICK RD. PENRYN, CORWALL TR 10 9DQ GB Other 510(k) Applications for this Company
Contact	BEN MURDOCK Other 510(k) Applications for this Contact
Regulation Number	884.6150   More FDA Info for this Regulation Number
Classification Product Code	MQJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/10/2000
Decision Date	11/22/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review