FDA 510(k) Application Details - K173545

Device Classification Name	Insufflator, Laparoscopic   More FDA Info for this Device
510(K) Number	K173545
Device Name	Insufflator, Laparoscopic
Applicant	TEMED Unit 3, Keynor Farm Sidlesham PO20 7LL GB Other 510(k) Applications for this Company
Contact	Katie Evans 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	11/16/2017
Decision Date	02/14/2018
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