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FDA 510(k)

THE SUN BOOTH

K-Number: K801095 · 1980-07-21

ApplicantSun Booths , Ltd.
Decision Date1980-07-21
Product CodeLEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE SUN BOOTH is the device name listed in this FDA 510(k) record. The listed applicant is Sun Booths , Ltd.. It received FDA 510(k) clearance on 1980-07-21 under 510(k) number K801095. 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 THE SUN BOOTH?

THE SUN BOOTH is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is Sun Booths , Ltd.. The 510(k) number is K801095.

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

THE SUN BOOTH received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801095.

Who is the listed applicant for THE SUN BOOTH?

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

What is the FDA product code for THE SUN BOOTH?

The FDA product code for THE SUN BOOTH 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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