510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K223775Substantially Equivalent

EZ-STIK Electrodes

South Dakota Partners, Clear Lake SD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K223775 is the FDA 510(k) clearance record for EZ-STIK Electrodes, a class II device, cleared for South Dakota Partners on under FDA product code GXY (Electrode, Cutaneous). FDA records list one 510(k) clearance for South Dakota Partners. As of , FDA records show no recalls naming K223775.

Clearance record

Decision date
Received
(18 days to decision)
Product code
GXY Electrode, Cutaneous
Regulation
21 CFR 882.1320
Device class
Class II
Review panel
Neurology
Applicant
South Dakota Partners 205 Hwy. 22 E, Clear Lake SD
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code GXY

Trailing 12 months
11 clearances under product code GXY in the twelve months to October 2026, May 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code GXY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20261
April 20262
May 20263
June 20262
July 20261
August 20261
September 20260
October 20260