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FDA 510(k)

CABANNA TAN SUNLAMP

K-Number: K801925 · 1980-10-03

ApplicantThe Marketing Exchange, Inc.
Decision Date1980-10-03
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CABANNA TAN SUNLAMP is the device name listed in this FDA 510(k) record. The listed applicant is The Marketing Exchange, Inc.. It received FDA 510(k) clearance on 1980-10-03 under 510(k) number K801925. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CABANNA TAN SUNLAMP?

CABANNA TAN SUNLAMP is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is The Marketing Exchange, Inc.. The 510(k) number is K801925.

When did CABANNA TAN SUNLAMP receive FDA 510(k) clearance?

CABANNA TAN SUNLAMP received FDA 510(k) clearance on 1980-10-03, under 510(k) number K801925.

Who is the listed applicant for CABANNA TAN SUNLAMP?

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

What is the FDA product code for CABANNA TAN SUNLAMP?

The FDA product code for CABANNA TAN SUNLAMP is LEJ.

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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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