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FDA 510(k)

VINTAGE LD

K-Number: K152392 · 2016-01-08

ApplicantShofu Dental Corporation
Decision Date2016-01-08
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VINTAGE LD is a medical device manufactured by Shofu Dental Corporation. It received FDA 510(k) clearance on 2016-01-08 under approval number K152392. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VINTAGE LD?

VINTAGE LD is a medical device that received FDA 510(k) clearance on 2016-01-08. It is manufactured by Shofu Dental Corporation. The 510(k) number is K152392.

When was VINTAGE LD approved by the FDA?

VINTAGE LD received FDA 510(k) clearance on 2016-01-08, under approval number K152392.

What company makes VINTAGE LD?

VINTAGE LD is manufactured by Shofu Dental Corporation.

What is the FDA product code for VINTAGE LD?

The FDA product code for VINTAGE LD is EIH.

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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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