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FDA 510(k)

MXR-14 FILM PROCESSOR

K-Number: K890486 · 1990-04-03

ApplicantCordell, Inc.
Decision Date1990-04-03
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MXR-14 FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Cordell, Inc.. It received FDA 510(k) clearance on 1990-04-03 under 510(k) number K890486. 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 MXR-14 FILM PROCESSOR?

MXR-14 FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1990-04-03. The listed applicant is Cordell, Inc.. The 510(k) number is K890486.

When did MXR-14 FILM PROCESSOR receive FDA 510(k) clearance?

MXR-14 FILM PROCESSOR received FDA 510(k) clearance on 1990-04-03, under 510(k) number K890486.

Who is the listed applicant for MXR-14 FILM PROCESSOR?

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

What is the FDA product code for MXR-14 FILM PROCESSOR?

The FDA product code for MXR-14 FILM PROCESSOR is IXW.

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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

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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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