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FDA 510(k)

JPI AUTOMATIC X-RAY FILM PROCESSOR

K-Number: K955706 · 1996-02-12

ApplicantJpi Healthcare Co, Ltd.
Decision Date1996-02-12
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

JPI AUTOMATIC X-RAY FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Jpi Healthcare Co, Ltd.. It received FDA 510(k) clearance on 1996-02-12 under 510(k) number K955706. 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 JPI AUTOMATIC X-RAY FILM PROCESSOR?

JPI AUTOMATIC X-RAY FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1996-02-12. The listed applicant is Jpi Healthcare Co, Ltd.. The 510(k) number is K955706.

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

JPI AUTOMATIC X-RAY FILM PROCESSOR received FDA 510(k) clearance on 1996-02-12, under 510(k) number K955706.

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

The FDA 510(k) record lists Jpi Healthcare Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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

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Other records listing Jpi Healthcare Co, Ltd. 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.

K260482DRE DuoK244010ExamVue ApexK213057ExamVue DuoK102327CLEARVISION DR 7000FK101779CLEARVISION DR 2000 DIGITAL RADIOGRAPHY X-RAY SYSTEMK954161JPI INTENSIFYING SCREEN

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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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