KOSMEDICO GMBH SUNLAMP PRODUCTS
K-Number: K840158 · 1984-04-24
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Device Summary
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
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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