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FDA 510(k)

KONICA LASER IMAGER, DRYPRO MODEL 751/752

K-Number: K013052 · 2002-01-16

ApplicantKonica Minolta Medical & Graphic, Inc.
Decision Date2002-01-16
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KONICA LASER IMAGER, DRYPRO MODEL 751/752 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 2002-01-16 under 510(k) number K013052. 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 KONICA LASER IMAGER, DRYPRO MODEL 751/752?

KONICA LASER IMAGER, DRYPRO MODEL 751/752 is a medical device that received FDA 510(k) clearance on 2002-01-16. The listed applicant is Konica Minolta Medical & Graphic, Inc.. The 510(k) number is K013052.

When did KONICA LASER IMAGER, DRYPRO MODEL 751/752 receive FDA 510(k) clearance?

KONICA LASER IMAGER, DRYPRO MODEL 751/752 received FDA 510(k) clearance on 2002-01-16, under 510(k) number K013052.

Who is the listed applicant for KONICA LASER IMAGER, DRYPRO MODEL 751/752?

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 KONICA LASER IMAGER, DRYPRO MODEL 751/752?

The FDA product code for KONICA LASER IMAGER, DRYPRO MODEL 751/752 is LMC.

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Other records listing Konica Minolta Medical & Graphic, 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.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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