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FDA 510(k)

MODIFIED BRONCHOSCOPE AND ACCESSORIES

K-Number: K933433 · 1993-11-01

ApplicantFujinon, Inc.
Decision Date1993-11-01
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODIFIED BRONCHOSCOPE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Fujinon, Inc.. It received FDA 510(k) clearance on 1993-11-01 under 510(k) number K933433. 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 MODIFIED BRONCHOSCOPE AND ACCESSORIES?

MODIFIED BRONCHOSCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1993-11-01. The listed applicant is Fujinon, Inc.. The 510(k) number is K933433.

When did MODIFIED BRONCHOSCOPE AND ACCESSORIES receive FDA 510(k) clearance?

MODIFIED BRONCHOSCOPE AND ACCESSORIES received FDA 510(k) clearance on 1993-11-01, under 510(k) number K933433.

Who is the listed applicant for MODIFIED BRONCHOSCOPE AND ACCESSORIES?

The FDA 510(k) record lists Fujinon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED BRONCHOSCOPE AND ACCESSORIES?

The FDA product code for MODIFIED BRONCHOSCOPE AND ACCESSORIES is EOQ.

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Other records listing Fujinon, Inc. 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.

K120446FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EG-530UR2 AND EG-530UT2K112391FUJINON COLONOSCOPESK102466FUJINON EPX-4440HD DIGITAL VIDEO PROCESSORK111243FUJINON ULTRASONIC PROCESSORK091773FUJINON STERILE OVERTUBESK090116FUJINON COLONOSCOPE FOR DOUBLE BALLOON ENTERSCOPY SYSTEM MODEL, EC-450B15

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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.

K261637Single-use Flexible BronchoscopeHunan Vathin Medical Instrument Co., Ltd.K260309Ambu® aScope™ 5 Broncho 2.7/1.2; Ambu® aScope™ 5 Broncho 4.2/2.2; Ambu® aScope™ 5 Broncho 4.2/2.2 Sampler SetAmbu A/SK2540263.8mm Slim ProVu Video Bronchoscope (090-02-0038U); 5.0mm Regular ProVu Video Bronchoscope (090-02-0050U); 6.0mm Large ProVu Video Bronchoscope (090-02-0060U); ProVu Video Bronchoscope 8 display (040-07-0082U)Flexicare Medical Limited.K260382MONARCH™ Platform (MON-000008)Auris Health, Inc.K254037LungFlow Airway CatheterFree Flow Medical, Inc.K253137FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840TFujifilm Corporation

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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