510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935840Substantially Equivalent

Tl 20W/12/rs & Tl 40W/12/rs

Philips Lighting Co., Somerset NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935840 is the FDA 510(k) clearance record for TL 20W/12/RS & TL 40W/12/RS, a class II device, cleared for Philips Lighting Co. on under FDA product code FTC (Light, Ultraviolet, Dermatological). FDA records list 7 510(k) clearances for Philips Lighting Co., from to . As of , FDA records show no recalls naming K935840.

Clearance record

Decision date
Received
(79 days to decision)
Product code
FTC Light, Ultraviolet, Dermatological
Regulation
21 CFR 878.4630
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Philips Lighting Co. 200 Franklin Sq. Dr., Somerset NJ
510(k) summary
Summary
Third party review
No

Clearances, product code FTC

Trailing 12 months
2 clearances under product code FTC in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FTC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260