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FDA 510(k)

SUN SCENE TAN BOOTH

K-Number: K800592 · 1980-06-04

ApplicantSun Scene International, Inc.
Decision Date1980-06-04
Product Code
DecisionSubstantially Equivalent

Device Summary

SUN SCENE TAN BOOTH is the device name listed in this FDA 510(k) record. The listed applicant is Sun Scene International, Inc.. It received FDA 510(k) clearance on 1980-06-04 under 510(k) number K800592. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUN SCENE TAN BOOTH?

SUN SCENE TAN BOOTH is a medical device that received FDA 510(k) clearance on 1980-06-04. The listed applicant is Sun Scene International, Inc.. The 510(k) number is K800592.

When did SUN SCENE TAN BOOTH receive FDA 510(k) clearance?

SUN SCENE TAN BOOTH received FDA 510(k) clearance on 1980-06-04, under 510(k) number K800592.

Who is the listed applicant for SUN SCENE TAN BOOTH?

The FDA 510(k) record lists Sun Scene International, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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.

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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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