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FDA 510(k)

FILM PROCESSOR, MODEL LIFE RAY PRO 2500

K-Number: K023825 · 2003-02-12

ApplicantS.A.I.E.P. S.R.L.
Decision Date2003-02-12
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FILM PROCESSOR, MODEL LIFE RAY PRO 2500 is the device name listed in this FDA 510(k) record. The listed applicant is S.A.I.E.P. S.R.L.. It received FDA 510(k) clearance on 2003-02-12 under 510(k) number K023825. 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 PROCESSOR, MODEL LIFE RAY PRO 2500?

FILM PROCESSOR, MODEL LIFE RAY PRO 2500 is a medical device that received FDA 510(k) clearance on 2003-02-12. The listed applicant is S.A.I.E.P. S.R.L.. The 510(k) number is K023825.

When did FILM PROCESSOR, MODEL LIFE RAY PRO 2500 receive FDA 510(k) clearance?

FILM PROCESSOR, MODEL LIFE RAY PRO 2500 received FDA 510(k) clearance on 2003-02-12, under 510(k) number K023825.

Who is the listed applicant for FILM PROCESSOR, MODEL LIFE RAY PRO 2500?

The FDA 510(k) record lists S.A.I.E.P. S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FILM PROCESSOR, MODEL LIFE RAY PRO 2500?

The FDA product code for FILM PROCESSOR, MODEL LIFE RAY PRO 2500 is IXW.

Related Clinical Trials

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.

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Other records listing S.A.I.E.P. S.R.L. 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.

K023801FILM PROCESSOR, MODEL LIFE RAY PRO 1000

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.K023613AX200 AUTOMATIC X-RAY FILM PROCESSOR, MODEL 6586.036Alphatek Corp.

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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