FDA 510(k) Application Details - K231003

Device Classification Name	Laparoscope, General & Plastic Surgery   More FDA Info for this Device
510(K) Number	K231003
Device Name	Laparoscope, General & Plastic Surgery
Applicant	Guangdong OptoMedic Technologies, Inc. Suite 503, Building A, Golden Valley Intellicreation Community, No. 2 Yonganbei Street Foshan 528200 CN Other 510(k) Applications for this Company
Contact	Weijuan Guo 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	04/07/2023
Decision Date	07/06/2023
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