Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K952694Substantially Equivalent

Co Breath Analysis Module & Monoxol II

Bacharach, Inc., Bethesda MD / Traditional, Substantially Equivalent

K952694 is the FDA 510(k) clearance record for CO BREATH ANALYSIS MODULE & MONOXOL II, a class II device, cleared for Bacharach, Inc. on under FDA product code CCJ (Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase). FDA records list one 510(k) clearance for Bacharach, Inc. As of , FDA records show no recalls naming K952694.

Clearance record

Decision date
Received
(229 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
Bacharach, Inc. 7475 Wisconsin Ave.,, Bethesda MD
510(k) summary
Summary
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