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FDA 510(k)

Fujifilm Ultrasonic Processor

K-Number: K200850 · 2020-07-06

ApplicantFujifilm Corporation
Decision Date2020-07-06
Product CodeFDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Fujifilm Ultrasonic Processor is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Corporation. It received FDA 510(k) clearance on 2020-07-06 under 510(k) number K200850. 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 Fujifilm Ultrasonic Processor?

Fujifilm Ultrasonic Processor is a medical device that received FDA 510(k) clearance on 2020-07-06. The listed applicant is Fujifilm Corporation. The 510(k) number is K200850.

When did Fujifilm Ultrasonic Processor receive FDA 510(k) clearance?

Fujifilm Ultrasonic Processor received FDA 510(k) clearance on 2020-07-06, under 510(k) number K200850.

Who is the listed applicant for Fujifilm Ultrasonic Processor?

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 Fujifilm Ultrasonic Processor?

The FDA product code for Fujifilm Ultrasonic Processor 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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