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FDA 510(k)

SONY UP-DF750 DIGITAL FILM IMAGER

K-Number: K083522 · 2009-01-09

ApplicantSony Electronics, Inc.
Decision Date2009-01-09
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONY UP-DF750 DIGITAL FILM IMAGER is the device name listed in this FDA 510(k) record. The listed applicant is Sony Electronics, Inc.. It received FDA 510(k) clearance on 2009-01-09 under 510(k) number K083522. 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 SONY UP-DF750 DIGITAL FILM IMAGER?

SONY UP-DF750 DIGITAL FILM IMAGER is a medical device that received FDA 510(k) clearance on 2009-01-09. The listed applicant is Sony Electronics, Inc.. The 510(k) number is K083522.

When did SONY UP-DF750 DIGITAL FILM IMAGER receive FDA 510(k) clearance?

SONY UP-DF750 DIGITAL FILM IMAGER received FDA 510(k) clearance on 2009-01-09, under 510(k) number K083522.

Who is the listed applicant for SONY UP-DF750 DIGITAL FILM IMAGER?

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

What is the FDA product code for SONY UP-DF750 DIGITAL FILM IMAGER?

The FDA product code for SONY UP-DF750 DIGITAL FILM IMAGER is LMC.

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Other records listing Sony Electronics, Inc. as applicant

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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.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare CorporationK061999DRY LASER IMAGER, DRYPRO MODEL 832Konica Minolta Medical & Graphic, Inc.

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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