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FDA 510(k)

LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2

K-Number: K183337 · 2019-05-29

Decision Date2019-05-29
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2 is a medical device manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH. It received FDA 510(k) clearance on 2019-05-29 under approval number K183337. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2?

LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2 is a medical device that received FDA 510(k) clearance on 2019-05-29. It is manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH. The 510(k) number is K183337.

When was LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2 approved by the FDA?

LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2 received FDA 510(k) clearance on 2019-05-29, under approval number K183337.

What company makes LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2?

LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2 is manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH.

What is the FDA product code for LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2?

The FDA product code for LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2 is EBG.

Other Devices by DMG Chemisch-Pharmazeutische Fabrik GmbH

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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.