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FDA 510(k)

DRY LASER IMAGER, DRYPRO MODEL 832

K-Number: K061999 · 2006-08-15

ApplicantKonica Minolta Medical & Graphic, Inc.
Decision Date2006-08-15
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DRY LASER IMAGER, DRYPRO MODEL 832 is the device name listed in this FDA 510(k) record. The listed applicant is Konica Minolta Medical & Graphic, Inc.. It received FDA 510(k) clearance on 2006-08-15 under 510(k) number K061999. 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 DRY LASER IMAGER, DRYPRO MODEL 832?

DRY LASER IMAGER, DRYPRO MODEL 832 is a medical device that received FDA 510(k) clearance on 2006-08-15. The listed applicant is Konica Minolta Medical & Graphic, Inc.. The 510(k) number is K061999.

When did DRY LASER IMAGER, DRYPRO MODEL 832 receive FDA 510(k) clearance?

DRY LASER IMAGER, DRYPRO MODEL 832 received FDA 510(k) clearance on 2006-08-15, under 510(k) number K061999.

Who is the listed applicant for DRY LASER IMAGER, DRYPRO MODEL 832?

The FDA 510(k) record lists Konica Minolta Medical & Graphic, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRY LASER IMAGER, DRYPRO MODEL 832?

The FDA product code for DRY LASER IMAGER, DRYPRO MODEL 832 is LMC.

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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.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

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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