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FDA 510(k)

GlideScope BFlex Single-Use Bronchoscope System

K-Number: K183256 · 2019-01-04

ApplicantVerathon Medical (Canada) Ulc
Decision Date2019-01-04
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

GlideScope BFlex Single-Use Bronchoscope System is the device name listed in this FDA 510(k) record. The listed applicant is Verathon Medical (Canada) Ulc. It received FDA 510(k) clearance on 2019-01-04 under 510(k) number K183256. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GlideScope BFlex Single-Use Bronchoscope System?

GlideScope BFlex Single-Use Bronchoscope System is a medical device that received FDA 510(k) clearance on 2019-01-04. The listed applicant is Verathon Medical (Canada) Ulc. The 510(k) number is K183256.

When did GlideScope BFlex Single-Use Bronchoscope System receive FDA 510(k) clearance?

GlideScope BFlex Single-Use Bronchoscope System received FDA 510(k) clearance on 2019-01-04, under 510(k) number K183256.

Who is the listed applicant for GlideScope BFlex Single-Use Bronchoscope System?

The FDA 510(k) record lists Verathon Medical (Canada) Ulc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GlideScope BFlex Single-Use Bronchoscope System?

The FDA product code for GlideScope BFlex Single-Use Bronchoscope System is EOQ.

Other records listing Verathon Medical (Canada) Ulc as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253696CFlex Cystoscope - Standard Deflection (0570-0455); CFlex Cystoscope - Reverse Deflection (0570-0456); CystoView Monitor (0570-0465)K230948BFlex™ 2 Slim 3.8 Single-Use BronchoscopeK211947GlideScope BFlex 2.8 Single-Use BronchoscopeK193488GlideScope BFlex 3.8 Single-Use BronchoscopeK191948GlideScope BFlex 5.8 Single-Use Bronchoscope

Related Devices (Code: EOQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260382MONARCH™ Platform (MON-000008)Auris Health, Inc.K254037LungFlow Airway CatheterFree Flow Medical, Inc.K253137FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840TFujifilm CorporationK260565SmartClip Delivery Catheter (ADR-1715)Elucent MedicalK252341EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-Q190); EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-H190 ); EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-1TH190)Olympus Medical Systems Corp.K260420LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG)MacroLux Medical Technology Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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