SOLAR-GOLD UV-A BY EOS
K-Number: K843902 · 1984-11-08
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Device Summary
Frequently Asked Questions
What is the SOLAR-GOLD UV-A BY EOS?
SOLAR-GOLD UV-A BY EOS is a medical device that received FDA 510(k) clearance on 1984-11-08. The listed applicant is Eos-Werke, Gunther GmbH. The 510(k) number is K843902.
When did SOLAR-GOLD UV-A BY EOS receive FDA 510(k) clearance?
SOLAR-GOLD UV-A BY EOS received FDA 510(k) clearance on 1984-11-08, under 510(k) number K843902.
Who is the listed applicant for SOLAR-GOLD UV-A BY EOS?
The FDA 510(k) record lists Eos-Werke, Gunther GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOLAR-GOLD UV-A BY EOS?
The FDA product code for SOLAR-GOLD UV-A BY EOS is FTC.
Related Clinical Trials
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: FTC)
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
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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