LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2
K-Number: K183337 · 2019-05-29
Device Summary
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
Related Devices (Code: EBG)
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.