FDA 510(k) Application Details - K050521

Device Classification Name	Catheter, Assisted Reproduction   More FDA Info for this Device
510(K) Number	K050521
Device Name	Catheter, Assisted Reproduction
Applicant	INNTEC, INC. 800 LEVANGER LANE STOUGHTON, WI 53589 US Other 510(k) Applications for this Company
Contact	Gary Syring Other 510(k) Applications for this Contact
Regulation Number	884.6110   More FDA Info for this Regulation Number
Classification Product Code	MQF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/01/2005
Decision Date	05/02/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review