FDA 510(k) Application Details - K213773

Device Classification Name	Colonoscope And Accessories, Flexible/Rigid   More FDA Info for this Device
510(K) Number	K213773
Device Name	Colonoscope And Accessories, Flexible/Rigid
Applicant	Bpendo, LLC 216 Foreman Circle Norman, OK 73069 US Other 510(k) Applications for this Company
Contact	Robert Holbrook Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FDF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/02/2021
Decision Date	07/21/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review