FDA 510(k) Application Details - K962683

Device Classification Name	Insufflator, Laparoscopic   More FDA Info for this Device
510(K) Number	K962683
Device Name	Insufflator, Laparoscopic
Applicant	DEKNATEL, INC. 49 PLAIN ST. NORTH ATTLEBORO, MA 02760 US Other 510(k) Applications for this Company
Contact	DIANE E MINEAR, RAC 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	07/10/1996
Decision Date	01/10/1997
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