510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K051178Substantially Equivalent

Mee-1000A Neuromaster

Nihon Kohden America Inc, Foothill CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K051178 is the FDA 510(k) clearance record for MEE-1000A NEUROMASTER, a class II device, cleared for Nihon Kohden America, Inc. on under FDA product code GWF (Stimulator, Electrical, Evoked Response). FDA records list 166 510(k) clearances for Nihon Kohden America, Inc., from to . As of , FDA records show one recall naming K051178.

Clearance record

Decision date
Received
(100 days to decision)
Product code
GWF Stimulator, Electrical, Evoked Response
Regulation
21 CFR 882.1870
Device class
Class II
Review panel
Neurology
Applicant
Nihon Kohden America, Inc. 90 Icon St., Foothill CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GWF

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