510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K801674Substantially Equivalent

Sun Room Tanning Booth

Sun Tan Enterprises, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K801674 is the FDA 510(k) clearance record for SUN ROOM TANNING BOOTH, a class II device, cleared for Sun Tan Enterprises, Inc. on under FDA product code LEJ (Booth, Sun Tan). FDA records list one 510(k) clearance for Sun Tan Enterprises, Inc. As of , FDA records show no recalls naming K801674.

Clearance record

Decision date
Received
(56 days to decision)
Product code
LEJ Booth, Sun Tan
Regulation
21 CFR 878.4635
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Sun Tan Enterprises, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LEJ

Trailing 12 months

FDA records hold no clearances under product code LEJ in the trailing twelve months.

FDA records show no clearances under product code LEJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LEJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260