Semi-Oval Modular Suntanning Booth

FDA 510(k) K802756 · Tannhut

Substantially Equivalent

510(k) numberK802756

Submission

Device name
Semi-Oval Modular Suntanning Booth
Applicant
Tannhut
Mchenry, IL, US
Received
November 5, 1980
Decision date
January 22, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LEJ – Booth, Sun Tan
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4635
Specialty
General, Plastic Surgery

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More from Lpi, Inc.

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Questions and answers

When was Semi-Oval Modular Suntanning Booth cleared by the FDA?

Semi-Oval Modular Suntanning Booth (K802756) received a 510(k) decision of Substantially Equivalent on January 22, 1981, 78 days after the submission was received.

What is the product code of K802756?

The FDA product code is LEJ – Booth, Sun Tan, a Class II (moderate risk) device regulated under 21 CFR 878.4635.