FDA 510(k)

VARO Plan

K-Number: K200078 · 2020-04-10

Applicant3D Industrial Imaging Co., Ltd.

Decision Date2020-04-10

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

VARO Plan is the device name listed in this FDA 510(k) record. The listed applicant is 3D Industrial Imaging Co., Ltd.. It received FDA 510(k) clearance on 2020-04-10 under 510(k) number K200078. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARO Plan?

VARO Plan is a medical device that received FDA 510(k) clearance on 2020-04-10. The listed applicant is 3D Industrial Imaging Co., Ltd.. The 510(k) number is K200078.

When did VARO Plan receive FDA 510(k) clearance?

VARO Plan received FDA 510(k) clearance on 2020-04-10, under 510(k) number K200078.

Who is the listed applicant for VARO Plan?

The FDA 510(k) record lists 3D Industrial Imaging Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARO Plan?

The FDA product code for VARO Plan is LLZ.

Other records listing 3D Industrial Imaging Co., Ltd. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.