Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K833739Substantially Equivalent

Cd-102 Carbon Dioxide Analyzer/recor

Instrumentarium Corp., Tewksbury MA / Traditional, Substantially Equivalent

K833739 is the FDA 510(k) clearance record for CD-102 CARBON DIOXIDE ANALYZER/RECOR, a class II device, cleared for Instrumentarium Corp. on under FDA product code CCJ (Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase). FDA records list 20 510(k) clearances for Instrumentarium Corp., from to . As of , FDA records show no recalls naming K833739.

Clearance record

Decision date
Received
(52 days to decision)
Product code
CCJ Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase
Regulation
21 CFR 868.1430
Device class
Class II
Review panel
Anesthesiology
Applicant
Instrumentarium Corp. 2 Highwood Dr., Tewksbury MA
Third party review
No

Clearances, product code CCJ

Trailing 12 months
1 clearance under product code CCJ 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 CCJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260