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FDA 510(k)

UP-DF500 FILMSTATION DIGITAL FILM IMAGER

K-Number: K024188 · 2003-02-04

ApplicantSony Medical Systems
Decision Date2003-02-04
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UP-DF500 FILMSTATION DIGITAL FILM IMAGER is the device name listed in this FDA 510(k) record. The listed applicant is Sony Medical Systems. It received FDA 510(k) clearance on 2003-02-04 under 510(k) number K024188. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UP-DF500 FILMSTATION DIGITAL FILM IMAGER?

UP-DF500 FILMSTATION DIGITAL FILM IMAGER is a medical device that received FDA 510(k) clearance on 2003-02-04. The listed applicant is Sony Medical Systems. The 510(k) number is K024188.

When did UP-DF500 FILMSTATION DIGITAL FILM IMAGER receive FDA 510(k) clearance?

UP-DF500 FILMSTATION DIGITAL FILM IMAGER received FDA 510(k) clearance on 2003-02-04, under 510(k) number K024188.

Who is the listed applicant for UP-DF500 FILMSTATION DIGITAL FILM IMAGER?

The FDA 510(k) record lists Sony Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UP-DF500 FILMSTATION DIGITAL FILM IMAGER?

The FDA product code for UP-DF500 FILMSTATION DIGITAL FILM IMAGER is LMC.

Related Clinical Trials

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Other records listing Sony Medical Systems 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.

K970999SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITORK961680SONY DKR-700 DIGITAL STILL RECORDERK931170SONY CARDIAC ANALYSIS AND REVIEW STATION (CARS)K924708CINENET CARDIAC IMAGE NETWORKK921275SONY LASER VIDEODISC RECORDING SYSTEM

Related Devices (Code: LMC)

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.

K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation

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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