FDA 510(k) Application Details - K201617

Device Classification Name	Laparoscope, Gynecologic (And Accessories)   More FDA Info for this Device
510(K) Number	K201617
Device Name	Laparoscope, Gynecologic (And Accessories)
Applicant	Schoelly Fiberoptic GmbH Robert-Bosch-Strasse 1-3 Denzlingen 79211 DE Other 510(k) Applications for this Company
Contact	Sandra Baumann 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	06/15/2020
Decision Date	03/12/2021
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