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FDA 510(k)

FUJIFILM Endoscope Model EB-710P

K-Number: K220957 · 2022-11-10

ApplicantFujifilm Corporaton
Decision Date2022-11-10
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FUJIFILM Endoscope Model EB-710P is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Corporaton. It received FDA 510(k) clearance on 2022-11-10 under 510(k) number K220957. 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 FUJIFILM Endoscope Model EB-710P?

FUJIFILM Endoscope Model EB-710P is a medical device that received FDA 510(k) clearance on 2022-11-10. The listed applicant is Fujifilm Corporaton. The 510(k) number is K220957.

When did FUJIFILM Endoscope Model EB-710P receive FDA 510(k) clearance?

FUJIFILM Endoscope Model EB-710P received FDA 510(k) clearance on 2022-11-10, under 510(k) number K220957.

Who is the listed applicant for FUJIFILM Endoscope Model EB-710P?

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

What is the FDA product code for FUJIFILM Endoscope Model EB-710P?

The FDA product code for FUJIFILM Endoscope Model EB-710P is EOQ.

Other records listing Fujifilm Corporaton 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.

K221551FUJIFILM Endoscope Model EI-740D/SK223295Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500DK212950FUJIFILM Video Laparoscope EL-R740M30K203717Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0K200973Synapse 3D Cardiac Tools

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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