FDA 510(k)

FILM-X 90

K-Number: K790121 · 1979-02-21

Decision Date1979-02-21

Product CodeIXW

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

FILM-X 90 is the device name listed in this FDA 510(k) record. The listed applicant is Automatic Film Processor Corp.. It received FDA 510(k) clearance on 1979-02-21 under 510(k) number K790121. 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 FILM-X 90?

FILM-X 90 is a medical device that received FDA 510(k) clearance on 1979-02-21. The listed applicant is Automatic Film Processor Corp.. The 510(k) number is K790121.

When did FILM-X 90 receive FDA 510(k) clearance?

FILM-X 90 received FDA 510(k) clearance on 1979-02-21, under 510(k) number K790121.

Who is the listed applicant for FILM-X 90?

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

What is the FDA product code for FILM-X 90?

The FDA product code for FILM-X 90 is IXW.

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. KG K024342RADIOGRAPHIC 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.