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FDA 510(k)

FUJI DAYLIGHT CASSETTE MULTI-LOADER

K-Number: K933408 · 1993-08-16

ApplicantFujifilm Medical System U.S.A., Inc.
Decision Date1993-08-16
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FUJI DAYLIGHT CASSETTE MULTI-LOADER 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 1993-08-16 under 510(k) number K933408. 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 FUJI DAYLIGHT CASSETTE MULTI-LOADER?

FUJI DAYLIGHT CASSETTE MULTI-LOADER is a medical device that received FDA 510(k) clearance on 1993-08-16. The listed applicant is Fujifilm Medical System U.S.A., Inc.. The 510(k) number is K933408.

When did FUJI DAYLIGHT CASSETTE MULTI-LOADER receive FDA 510(k) clearance?

FUJI DAYLIGHT CASSETTE MULTI-LOADER received FDA 510(k) clearance on 1993-08-16, under 510(k) number K933408.

Who is the listed applicant for FUJI DAYLIGHT CASSETTE MULTI-LOADER?

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 DAYLIGHT CASSETTE MULTI-LOADER?

The FDA product code for FUJI DAYLIGHT CASSETTE MULTI-LOADER is IXW.

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Other records listing Fujifilm Medical System U.S.A., Inc. as applicant

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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

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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