Cleared Traditional

Ambu? aScope? 5 Broncho HD 5.0/2.2, Ambu? aScope? 5 Broncho HD 5.6/2.8, Ambu? aView? 2 Advance

K223299 · Ambu A/S · Ear, Nose, Throat

Jun 2023

Decision

217d

Days

Class 2

Risk

About This 510(k) Submission

K223299 is an FDA 510(k) clearance for the Ambu? aScope? 5 Broncho HD 5.0/2.2, Ambu? aScope? 5 Broncho HD 5.6/2.8, Ambu? aView? 2 Advance, a Bronchoscope (flexible Or Rigid) (Class II — Special Controls, product code EOQ), submitted by Ambu A/S (Ballerup, DK). The FDA issued a Cleared decision on June 1, 2023, 217 days after receiving the submission on October 27, 2022. This device falls under the Ear, Nose, Throat review panel. Regulated under 21 CFR 874.4680.

Submission Details

510(k) Number	K223299 FDA.gov
FDA Decision	Cleared SESE
Date Received	October 27, 2022
Decision Date	June 01, 2023
Days to Decision	217 days
Submission Type	Traditional
Review Panel	Ear, Nose, Throat (EN)
Summary	Summary PDF

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).