FDA 510(k) Application Details - K003703

Device Classification Name	Insufflator, Laparoscopic   More FDA Info for this Device
510(K) Number	K003703
Device Name	Insufflator, Laparoscopic
Applicant	TAUT, INC. 2571 KANEVILLE COURT GENEVA, IL 60134 US Other 510(k) Applications for this Company
Contact	RONALD KENSETH Other 510(k) Applications for this Contact
Regulation Number	884.1730   More FDA Info for this Regulation Number
Classification Product Code	HIF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/01/2000
Decision Date	02/22/2001
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