Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K243956Substantially Equivalent

TG-980P CO2 Sensor Kit (TG-980P); TG-980P1 CO2 Sensor Kit (TG-980P1)

Nihon Kohden Corp., Tokyo, JP / Traditional, Substantially Equivalent

K243956 is the FDA 510(k) clearance record for TG-980P CO2 Sensor Kit (TG-980P); TG-980P1 CO2 Sensor Kit (TG-980P1), a class II device, cleared for Nihon Kohden Corporation on under FDA product code CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). FDA records list 31 510(k) clearances for Nihon Kohden Corporation, from to . As of , FDA records show no recalls naming K243956.

Clearance record

Decision date
Received
(169 days to decision)
Product code
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Regulation
21 CFR 868.1400
Device class
Class II
Review panel
Anesthesiology
Applicant
Nihon Kohden Corporation 1-31-4 Nishiochiai, Shinjuku-Ku, Tokyo, JP
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CCK

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