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FDA 510(k)

FUJI EC ID CAMERA

K-Number: K932357 · 1993-07-26

ApplicantFujifilm Medical System U.S.A., Inc.
Decision Date1993-07-26
Product CodeJAC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FUJI EC ID CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Medical System U.S.A., Inc.. It received FDA 510(k) clearance on 1993-07-26 under 510(k) number K932357. The device is classified under product code JAC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJI EC ID CAMERA?

FUJI EC ID CAMERA is a medical device that received FDA 510(k) clearance on 1993-07-26. The listed applicant is Fujifilm Medical System U.S.A., Inc.. The 510(k) number is K932357.

When did FUJI EC ID CAMERA receive FDA 510(k) clearance?

FUJI EC ID CAMERA received FDA 510(k) clearance on 1993-07-26, under 510(k) number K932357.

Who is the listed applicant for FUJI EC ID CAMERA?

The FDA 510(k) record lists Fujifilm Medical System U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FUJI EC ID CAMERA?

The FDA product code for FUJI EC ID CAMERA is JAC.

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Other records listing Fujifilm Medical System U.S.A., 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.

K163675Processor VP-7000, Light Source BL-7000K153206Fujifilm Ultrasonic Processors SU-1 PLATINUM and SU-1K151474Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter)K132188MAMMOGRAPHY VIEWER SMV658K130542SYNAPSE 3D LUNG AND ABDOMEN ANALYSISK130383SYNAPSE 3D CARDIAC TOOLS

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Related Devices (Code: JAC)

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.

K942883DIGITAL I.D. CAMERAMiles Inc., Agfa DivisionK930752CT/MRI TOPOGRAPHIC MARKERI.Z.I. Corp.K925892SOLSTICE XRAY RING MARKER PADSolstice Corp.K926404KODAK X-OMATIC IDENTIFICATION CAMERA, MODEL 4 & 4LEastman Kodak CompanyK923533ADMARKPlanmeca USA, Inc.K925332BENNETT X-RAY ID PLUSBennett X-Ray Technologies

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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