Cleared Traditional

Vathin? Video Bronchoscope System

K223836 · Hunan Vathin Medical Instrument Co., Ltd. · Ear, Nose, Throat

May 2023

Decision

144d

Days

Class 2

Risk

About This 510(k) Submission

K223836 is an FDA 510(k) clearance for the Vathin? Video Bronchoscope System, a Bronchoscope (flexible Or Rigid) (Class II — Special Controls, product code EOQ), submitted by Hunan Vathin Medical Instrument Co., Ltd. (Xiangtan, CN). The FDA issued a Cleared decision on May 15, 2023, 144 days after receiving the submission on December 22, 2022. This device falls under the Ear, Nose, Throat review panel. Regulated under 21 CFR 874.4680.

Submission Details

510(k) Number	K223836 FDA.gov
FDA Decision	Cleared SESE
Date Received	December 22, 2022
Decision Date	May 15, 2023
Days to Decision	144 days
Submission Type	Traditional
Review Panel	Ear, Nose, Throat (EN)
Summary	Statement

Device Classification

Product Code	EOQ — Bronchoscope (flexible Or Rigid)
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 874.4680
Definition	A Bronchoscope (flexible Or Rigid) And Accessories Is A Tubular Endoscopic Device With Any Of A Group Of Accessory Devices Which Attach To The Bronchoscope And Is Intended To Examine Or Treat The Larynx And Tracheobronchial Tree. If The Device Is Reprocessed, Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission. If The Device Is Reusable, Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).