510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K043586Substantially Equivalent

Laser Sys*stim 540, Model Me 540

Mettler Electronics Corp, Anaheim CA / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K043586 is the FDA 510(k) clearance record for LASER SYS*STIM 540, MODEL ME 540, a class II device, cleared for Mettler Electronics Corp. on under FDA product code ILY (Lamp, Infrared, Therapeutic Heating). FDA records list 34 510(k) clearances for Mettler Electronics Corp., from to . As of , FDA records show no recalls naming K043586.

Clearance record

Decision date
Received
(129 days to decision)
Product code
ILY Lamp, Infrared, Therapeutic Heating
Regulation
21 CFR 890.5500
Device class
Class II
Review panel
Physical Medicine
Applicant
Mettler Electronics Corp. 1333 S. Claudina St., Anaheim CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ILY

Trailing 12 months
1 clearance under product code ILY 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 ILY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260