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FDA 510(k)

RADIOGRAPHIC FILM MARKETING SYSTEM

K-Number: K924345 · 1992-11-27

ApplicantFischer Imaging Corp.
Decision Date1992-11-27
Product CodeJAC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIOGRAPHIC FILM MARKETING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Fischer Imaging Corp.. It received FDA 510(k) clearance on 1992-11-27 under 510(k) number K924345. 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 RADIOGRAPHIC FILM MARKETING SYSTEM?

RADIOGRAPHIC FILM MARKETING SYSTEM is a medical device that received FDA 510(k) clearance on 1992-11-27. The listed applicant is Fischer Imaging Corp.. The 510(k) number is K924345.

When did RADIOGRAPHIC FILM MARKETING SYSTEM receive FDA 510(k) clearance?

RADIOGRAPHIC FILM MARKETING SYSTEM received FDA 510(k) clearance on 1992-11-27, under 510(k) number K924345.

Who is the listed applicant for RADIOGRAPHIC FILM MARKETING SYSTEM?

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

What is the FDA product code for RADIOGRAPHIC FILM MARKETING SYSTEM?

The FDA product code for RADIOGRAPHIC FILM MARKETING SYSTEM is JAC.

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Other records listing Fischer Imaging Corp. 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.

K042095MAMMOTESTK021113MAMMOPATHK981414LC POSITIONERK973400MAMMOTEST ADAPTER DRIVERK964806MD-1835K961207EP-X BIPLANE

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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.K932357FUJI EC ID CAMERAFujifilm Medical System U.S.A., Inc.K925892SOLSTICE XRAY RING MARKER PADSolstice Corp.K926404KODAK X-OMATIC IDENTIFICATION CAMERA, MODEL 4 & 4LEastman Kodak CompanyK923533ADMARKPlanmeca USA, 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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