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FDA 510(k)

CARESTREAM DRYVIEW 5850 LASER IMAGER

K-Number: K090469 · 2009-05-22

ApplicantCarestream Health, Inc.
Decision Date2009-05-22
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CARESTREAM DRYVIEW 5850 LASER IMAGER is the device name listed in this FDA 510(k) record. The listed applicant is Carestream Health, Inc.. It received FDA 510(k) clearance on 2009-05-22 under 510(k) number K090469. 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 CARESTREAM DRYVIEW 5850 LASER IMAGER?

CARESTREAM DRYVIEW 5850 LASER IMAGER is a medical device that received FDA 510(k) clearance on 2009-05-22. The listed applicant is Carestream Health, Inc.. The 510(k) number is K090469.

When did CARESTREAM DRYVIEW 5850 LASER IMAGER receive FDA 510(k) clearance?

CARESTREAM DRYVIEW 5850 LASER IMAGER received FDA 510(k) clearance on 2009-05-22, under 510(k) number K090469.

Who is the listed applicant for CARESTREAM DRYVIEW 5850 LASER IMAGER?

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

What is the FDA product code for CARESTREAM DRYVIEW 5850 LASER IMAGER?

The FDA product code for CARESTREAM DRYVIEW 5850 LASER IMAGER is LMC.

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Other records listing Carestream Health, 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.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, 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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