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FDA 510(k)

VERAVIEWEPOCS, MODEL VE

K-Number: K013955 · 2002-02-04

ApplicantJ. Morita USA, Inc.
Decision Date2002-02-04
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VERAVIEWEPOCS, MODEL VE 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 2002-02-04 under 510(k) number K013955. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERAVIEWEPOCS, MODEL VE?

VERAVIEWEPOCS, MODEL VE is a medical device that received FDA 510(k) clearance on 2002-02-04. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K013955.

When did VERAVIEWEPOCS, MODEL VE receive FDA 510(k) clearance?

VERAVIEWEPOCS, MODEL VE received FDA 510(k) clearance on 2002-02-04, under 510(k) number K013955.

Who is the listed applicant for VERAVIEWEPOCS, MODEL VE?

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 VERAVIEWEPOCS, MODEL VE?

The FDA product code for VERAVIEWEPOCS, MODEL VE is EHD.

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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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