FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DiLumen C2 and Tool Mount

K Number: K211819 · Decision Oct 22, 2021
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
108
Applicant Total
8
Review Days
133

Basic Information

Device Name
DiLumen C2 and Tool Mount
K Number
K211819
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lumendi, LLC
Date Received
June 11, 2021
Decision Date
October 22, 2021
Product Code
FDF
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FDF Colonoscope And Accessories, Flexible/Rigid

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Other Clearances by Lumendi, LLC

K Number Device Name
K221452 DiLumen C1, EZ1 and Tool Mount
K210851 DiLumen Endolumenal Interventional Platform (DiLumen)
K183112 DiLumen Endolumenal Interventional Knife (“DiLumen IK™”)
K182540 DiLumen Endolumenal Interventional Platform
K173405 DiLumen Endolumenal Interventional Scissors (DiLumen Is)
K173317 DiLumen C2; DiLumen Tool Mount
K162428 DiLumen Endolumenal Interventional Platform