510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850342Substantially Equivalent for Some Indications

Wyler Subdural Strip Electrode

AD-Tech Medical Instrument Corp., Racine WI / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K850342 is the FDA 510(k) clearance record for WYLER SUBDURAL STRIP ELECTRODE, a class II device, cleared for Ad-Tech Medical Instrument Corp on under FDA product code GYC (Electrode, Cortical). FDA records list 26 510(k) clearances for Ad-Tech Medical Instrument Corp, from to . As of , FDA records show no recalls naming K850342.

Clearance record

Decision date
Received
(183 days to decision)
Product code
GYC Electrode, Cortical
Regulation
21 CFR 882.1310
Device class
Class II
Review panel
Neurology
Applicant
Ad-Tech Medical Instrument Corp 1901 William St.,, Racine WI
Third party review
No

Clearances, product code GYC

Trailing 12 months

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

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