510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K142567Substantially Equivalent

RETeval Visual Electrodiagnostic Device

LKC Technologies, Inc., Gaithersburg MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K142567 is the FDA 510(k) clearance record for RETeval Visual Electrodiagnostic Device, a class II device, cleared for Lkc Technologies, Inc. on under FDA product code GWE (Stimulator, Photic, Evoked Response). FDA records list 8 510(k) clearances for Lkc Technologies, Inc., from to . As of , FDA records show no recalls naming K142567.

Clearance record

Decision date
Received
(249 days to decision)
Product code
GWE Stimulator, Photic, Evoked Response
Regulation
21 CFR 882.1890
Device class
Class II
Review panel
Neurology
Applicant
Lkc Technologies, Inc. 2 Professional Dr., Suite 222, Gaithersburg MD
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GWE

Trailing 12 months

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

FDA records show no clearances under product code GWE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GWE, 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