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FDA 510(k)

FREEDOM AUTOMATIC FILM PROCESSOR

K-Number: K002640 · 2000-11-08

ApplicantJ. Morita USA, Inc.
Decision Date2000-11-08
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FREEDOM AUTOMATIC FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 2000-11-08 under 510(k) number K002640. 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 FREEDOM AUTOMATIC FILM PROCESSOR?

FREEDOM AUTOMATIC FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 2000-11-08. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K002640.

When did FREEDOM AUTOMATIC FILM PROCESSOR receive FDA 510(k) clearance?

FREEDOM AUTOMATIC FILM PROCESSOR received FDA 510(k) clearance on 2000-11-08, under 510(k) number K002640.

Who is the listed applicant for FREEDOM AUTOMATIC FILM PROCESSOR?

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

What is the FDA product code for FREEDOM AUTOMATIC FILM PROCESSOR?

The FDA product code for FREEDOM AUTOMATIC FILM PROCESSOR is IXW.

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Other records listing J. Morita USA, 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.

K213477Root ZX3K2013783D Accuitomo 150NK190509Lubrina 2K173920LS OILK171012Veraview X800K170275Tri Auto ZX2

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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.K023825FILM PROCESSOR, MODEL LIFE RAY PRO 2500S.A.I.E.P. S.R.L.K023801FILM PROCESSOR, MODEL LIFE RAY PRO 1000S.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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