Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K853394Substantially Equivalent

600/L 5X6' Uva 85W Lamps, 5X5 Uva 65W Lamps 500/L

Interlab(Electromechanical), London,Nw11 8nd, England, GB / Traditional, Substantially Equivalent

K853394 is the FDA 510(k) clearance record for 600/L 5X6' UVA 85W LAMPS, 5X5 UVA 65W LAMPS 500/L, a class II device, cleared for Interlab(Electromechanical) on under FDA product code FTC (Light, Ultraviolet, Dermatological). FDA records list one 510(k) clearance for Interlab(Electromechanical). As of , FDA records show no recalls naming K853394.

Clearance record

Decision date
Received
(32 days to decision)
Product code
FTC Light, Ultraviolet, Dermatological
Regulation
21 CFR 878.4630
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Interlab(Electromechanical) 24 Helenslea Ave., London,Nw11 8nd, England, GB
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