FDA 510(k) Application Details - K141902

Device Classification Name	Laparoscope, General & Plastic Surgery   More FDA Info for this Device
510(K) Number	K141902
Device Name	Laparoscope, General & Plastic Surgery
Applicant	LAGIS ENTERPRISES CO, LTD. NO. 29, GONG 1ST RD., DAJIA TAICHUNG 437 TW Other 510(k) Applications for this Company
Contact	CORA CHEN Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	GCJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/14/2014
Decision Date	05/26/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review