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. The listed applicant is DMG Chemisch-Pharmazeutische Fabrik GmbH. The 510(k) number is K183337.
When did LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2 receive FDA 510(k) clearance?
LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2 received FDA 510(k) clearance on 2019-05-29, under 510(k) number K183337.
Who is the listed applicant for LuxaCrown, Shade A1, A2, A3, A3.5; LuxaCrown B1, B3, C2, D2?
The FDA 510(k) record lists DMG Chemisch-Pharmazeutische Fabrik GmbH as the applicant. This does not by itself establish the device manufacturer.
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 records listing DMG Chemisch-Pharmazeutische Fabrik GmbH as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EBG)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
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