510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K010084Substantially Equivalent

Real Patient Real Patient 128 Channel EEG Headbox, Model Ex-Nw-128-Rp

Excel Tech., Ltd., Oakville, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K010084 is the FDA 510(k) clearance record for REAL PATIENT REAL PATIENT 128 CHANNEL EEG HEADBOX, MODEL EX-NW-128-RP, a class II device, cleared for Excel Tech. , Ltd. on under FDA product code GWQ (Full-Montage Standard Electroencephalograph). FDA's definition for product code GWQ reads: "Acquire, display, store, and archive electroencephalographic signals from the brain using a full montage array (i.e., 16 or more electrodes) and user-specified locations". FDA records list 58 510(k) clearances for Excel Tech. , Ltd., from to . As of , FDA records show no recalls naming K010084.

Clearance record

Decision date
Received
(64 days to decision)
Product code
GWQ Full-Montage Standard Electroencephalograph
Regulation
21 CFR 882.1400
Device class
Class II
Review panel
Neurology
Applicant
Excel Tech. , Ltd. 2568 Bristol Cir., Oakville, CA
510(k) summary
Summary
Third party review
No

Clearances, product code GWQ

Trailing 12 months
2 clearances under product code GWQ in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GWQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260