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FDA 510(k)

SUNTANNING BOOTH

K-Number: K827666 · 1982-07-22

ApplicantCarribean Connection
Decision Date1982-07-22
Product Code
DecisionSubstantially Equivalent

Device Summary

SUNTANNING BOOTH is the device name listed in this FDA 510(k) record. The listed applicant is Carribean Connection. It received FDA 510(k) clearance on 1982-07-22 under 510(k) number K827666. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNTANNING BOOTH?

SUNTANNING BOOTH is a medical device that received FDA 510(k) clearance on 1982-07-22. The listed applicant is Carribean Connection. The 510(k) number is K827666.

When did SUNTANNING BOOTH receive FDA 510(k) clearance?

SUNTANNING BOOTH received FDA 510(k) clearance on 1982-07-22, under 510(k) number K827666.

Who is the listed applicant for SUNTANNING BOOTH?

The FDA 510(k) record lists Carribean Connection 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.

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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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