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FDA 510(k)

DIGITAL PRINTER P6000D SERIES, MODEL P6000DU

K-Number: K061302 · 2006-06-23

ApplicantMitsubishi Electric Corporation Kyoto Works
Decision Date2006-06-23
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL PRINTER P6000D SERIES, MODEL P6000DU is the device name listed in this FDA 510(k) record. The listed applicant is Mitsubishi Electric Corporation Kyoto Works. It received FDA 510(k) clearance on 2006-06-23 under 510(k) number K061302. 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 DIGITAL PRINTER P6000D SERIES, MODEL P6000DU?

DIGITAL PRINTER P6000D SERIES, MODEL P6000DU is a medical device that received FDA 510(k) clearance on 2006-06-23. The listed applicant is Mitsubishi Electric Corporation Kyoto Works. The 510(k) number is K061302.

When did DIGITAL PRINTER P6000D SERIES, MODEL P6000DU receive FDA 510(k) clearance?

DIGITAL PRINTER P6000D SERIES, MODEL P6000DU received FDA 510(k) clearance on 2006-06-23, under 510(k) number K061302.

Who is the listed applicant for DIGITAL PRINTER P6000D SERIES, MODEL P6000DU?

The FDA 510(k) record lists Mitsubishi Electric Corporation Kyoto Works as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL PRINTER P6000D SERIES, MODEL P6000DU?

The FDA product code for DIGITAL PRINTER P6000D SERIES, MODEL P6000DU is LMC.

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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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