510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K103140Substantially Equivalent

Nicolet Wireless EEG

Medtronic, Inc., Middleton WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K103140 is the FDA 510(k) clearance record for NICOLET WIRELESS EEG, a class II device, cleared for Carefusion 209, Inc. on under FDA product code GWL (Amplifier, Physiological Signal). FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show one recall naming K103140.

Clearance record

Decision date
Received
(165 days to decision)
Product code
GWL Amplifier, Physiological Signal
Regulation
21 CFR 882.1835
Device class
Class II
Review panel
Neurology
Applicant
Carefusion 209, Inc. 1850 Deming Way, Middleton WI
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code GWL

Trailing 12 months

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

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