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FDA 510(k)

WALDMANN SUNTANNING EQUIP-MODELS'S

K-Number: K840555 · 1984-05-23

ApplicantEurotan Intl.
Decision Date1984-05-23
Product Code
DecisionSubstantially Equivalent

Device Summary

WALDMANN SUNTANNING EQUIP-MODELS'S is the device name listed in this FDA 510(k) record. The listed applicant is Eurotan Intl.. It received FDA 510(k) clearance on 1984-05-23 under 510(k) number K840555. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALDMANN SUNTANNING EQUIP-MODELS'S?

WALDMANN SUNTANNING EQUIP-MODELS'S is a medical device that received FDA 510(k) clearance on 1984-05-23. The listed applicant is Eurotan Intl.. The 510(k) number is K840555.

When did WALDMANN SUNTANNING EQUIP-MODELS'S receive FDA 510(k) clearance?

WALDMANN SUNTANNING EQUIP-MODELS'S received FDA 510(k) clearance on 1984-05-23, under 510(k) number K840555.

Who is the listed applicant for WALDMANN SUNTANNING EQUIP-MODELS'S?

The FDA 510(k) record lists Eurotan Intl. as the applicant. This does not by itself establish the device manufacturer.

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 Eurotan Intl. 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.

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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