510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K841612Substantially Equivalent

Neuropack II 5100

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

K841612 is the FDA 510(k) clearance record for NEUROPACK II 5100, a class II device, cleared for Nihon Kohden America, Inc. on under FDA product code GWL (Amplifier, Physiological Signal). FDA records list 166 510(k) clearances for Nihon Kohden America, Inc., from to . As of , FDA records show no recalls naming K841612.

Clearance record

Decision date
Received
(58 days to decision)
Product code
GWL Amplifier, Physiological Signal
Regulation
21 CFR 882.1835
Device class
Class II
Review panel
Neurology
Applicant
Nihon Kohden America, Inc. 90 Icon St., Foothill CA
Third party review
No

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