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FDA 510(k)

Endoscope Model EI-740D/S

K-Number: K210162 · 2021-04-09

ApplicantFujifilm Corporation
Decision Date2021-04-09
Product CodeFDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Endoscope Model EI-740D/S is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Corporation. It received FDA 510(k) clearance on 2021-04-09 under 510(k) number K210162. The device is classified under product code FDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Endoscope Model EI-740D/S?

Endoscope Model EI-740D/S is a medical device that received FDA 510(k) clearance on 2021-04-09. The listed applicant is Fujifilm Corporation. The 510(k) number is K210162.

When did Endoscope Model EI-740D/S receive FDA 510(k) clearance?

Endoscope Model EI-740D/S received FDA 510(k) clearance on 2021-04-09, under 510(k) number K210162.

Who is the listed applicant for Endoscope Model EI-740D/S?

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

What is the FDA product code for Endoscope Model EI-740D/S?

The FDA product code for Endoscope Model EI-740D/S is FDS.

Other records listing Fujifilm Corporation 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.

K261170BA-004CCK260567EW10-EC02 Endoscopy Support ProgramK261880FUJIFILM Processor EP-8000;Balloon Controller PB-30;Endoscopy Support Program EW10-VM01K253137FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840TK254075Synapse Lung Nodule AIK254189Synapse 3D Base Tools (V7.2)

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Related Devices (Code: FDS)

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.

K253702Intuitive Endoluminal Gastrointestinal System (IG1000)Intuitive Surgical, Inc.K260573EvoEndo Single-Use Endoscopy SystemEvoEndo, Inc.K250550FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display UnitFujifilm CorporationK253568Hood DH-084STR; Hood DH-094STR; Hood DH-104STR; Hood DH-114STR; Hood DH-124STR; Hood DH-134STRFujifilm CorporationK251256PENTAX Medical Video Upper GI Scopes (EG Family) (EG Family); PENTAX Medical Video Colonoscopes (EC Family) (EC Family)Pentax of America, Inc.K251041GripTract-GI™ Endoscopic Tissue Manipulator Upper GI Model GT-GS100Actuated Medical, Inc.

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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