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FDA 510(k)

VERAVIEW IC 5, MODEL XDP1

K-Number: K053220 · 2006-01-06

ApplicantJ. Morita USA, Inc.
Decision Date2006-01-06
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VERAVIEW IC 5, MODEL XDP1 is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 2006-01-06 under 510(k) number K053220. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERAVIEW IC 5, MODEL XDP1?

VERAVIEW IC 5, MODEL XDP1 is a medical device that received FDA 510(k) clearance on 2006-01-06. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K053220.

When did VERAVIEW IC 5, MODEL XDP1 receive FDA 510(k) clearance?

VERAVIEW IC 5, MODEL XDP1 received FDA 510(k) clearance on 2006-01-06, under 510(k) number K053220.

Who is the listed applicant for VERAVIEW IC 5, MODEL XDP1?

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

What is the FDA product code for VERAVIEW IC 5, MODEL XDP1?

The FDA product code for VERAVIEW IC 5, MODEL XDP1 is MUH.

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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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