FDA 510(k) Application Details - K210104

Device Classification Name	Laparoscope, Gynecologic (And Accessories)   More FDA Info for this Device
510(K) Number	K210104
Device Name	Laparoscope, Gynecologic (And Accessories)
Applicant	270Surgical Ltd. 4 Arie Regev Street Netanya 4250212 IL Other 510(k) Applications for this Company
Contact	Avi Levy Other 510(k) Applications for this Contact
Regulation Number	884.1720   More FDA Info for this Regulation Number
Classification Product Code	HET Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/14/2021
Decision Date	07/08/2021
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