510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K931426Substantially Equivalent

Nf-11-E Disposable Reference/recording Electrode

Medicotest, Inc., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931426 is the FDA 510(k) clearance record for NF-11-E DISPOSABLE REFERENCE/RECORDING ELECTRODE, a class II device, cleared for Medicotest, Inc. on under FDA product code GXY (Electrode, Cutaneous). FDA records list 21 510(k) clearances for Medicotest, Inc., from to . As of , FDA records show no recalls naming K931426.

Clearance record

Decision date
Received
(274 days to decision)
Product code
GXY Electrode, Cutaneous
Regulation
21 CFR 882.1320
Device class
Class II
Review panel
Neurology
Applicant
Medicotest, Inc. One Metropolitan Sq., St. Louis MO
510(k) summary
Statement
Third party review
No

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