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FDA 510(k)

SOLAR-GOLD UV-A BY EOS

K-Number: K843902 · 1984-11-08

Decision Date1984-11-08
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SOLAR-GOLD UV-A BY EOS is the device name listed in this FDA 510(k) record. The listed applicant is Eos-Werke, Gunther GmbH. It received FDA 510(k) clearance on 1984-11-08 under 510(k) number K843902. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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