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FDA 510(k)

KOSMEDICO GMBH SUNLAMP PRODUCTS

K-Number: K840158 · 1984-04-24

Decision Date1984-04-24
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KOSMEDICO GMBH SUNLAMP PRODUCTS is the device name listed in this FDA 510(k) record. The listed applicant is Kosmedico, Kosmetische & Medizinisch. It received FDA 510(k) clearance on 1984-04-24 under 510(k) number K840158. 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 KOSMEDICO GMBH SUNLAMP PRODUCTS?

KOSMEDICO GMBH SUNLAMP PRODUCTS is a medical device that received FDA 510(k) clearance on 1984-04-24. The listed applicant is Kosmedico, Kosmetische & Medizinisch. The 510(k) number is K840158.

When did KOSMEDICO GMBH SUNLAMP PRODUCTS receive FDA 510(k) clearance?

KOSMEDICO GMBH SUNLAMP PRODUCTS received FDA 510(k) clearance on 1984-04-24, under 510(k) number K840158.

Who is the listed applicant for KOSMEDICO GMBH SUNLAMP PRODUCTS?

The FDA 510(k) record lists Kosmedico, Kosmetische & Medizinisch as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KOSMEDICO GMBH SUNLAMP PRODUCTS?

The FDA product code for KOSMEDICO GMBH SUNLAMP PRODUCTS 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.

Other records listing Kosmedico, Kosmetische & Medizinisch 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: 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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