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FDA 510(k)

C900 X-RAY FILM PROCESSOR

K-Number: K874908 · 1988-02-12

ApplicantSummit Industries, Inc.
Decision Date1988-02-12
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

C900 X-RAY FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Summit Industries, Inc.. It received FDA 510(k) clearance on 1988-02-12 under 510(k) number K874908. The device is classified under product code IXW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C900 X-RAY FILM PROCESSOR?

C900 X-RAY FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1988-02-12. The listed applicant is Summit Industries, Inc.. The 510(k) number is K874908.

When did C900 X-RAY FILM PROCESSOR receive FDA 510(k) clearance?

C900 X-RAY FILM PROCESSOR received FDA 510(k) clearance on 1988-02-12, under 510(k) number K874908.

Who is the listed applicant for C900 X-RAY FILM PROCESSOR?

The FDA 510(k) record lists Summit Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C900 X-RAY FILM PROCESSOR?

The FDA product code for C900 X-RAY FILM PROCESSOR is IXW.

Related Clinical Trials

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.

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Other records listing Summit Industries, 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.

K874687COLLI-MATETM MODEL NO. B800K851440RDIOGRAPHIC WALL HOLDER OR FILM RECEPTORK850198FLOOR TO WALL OR FLOOR TO CEILING TUBESTAND;RADIOGK850117XMA 325 (X-RAY GENERATOR)K850118XMA INTEGRATED TABLE

Related Devices (Code: IXW)

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.

K111167XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINTVelopex International, Inc.K093503INTRAX FILM PROCESSORVelopex International, Inc.K091628OPTIMAX, COMPACT 2, OPTIMAX 2010, ECOMAXProtec GmbH & Co. KGK024342RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000Daito Co., Ltd.K023801FILM PROCESSOR, MODEL LIFE RAY PRO 1000S.A.I.E.P. S.R.L.K023825FILM PROCESSOR, MODEL LIFE RAY PRO 2500S.A.I.E.P. S.R.L.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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