CAHClass II

Filter, Bacterial, Breathing-Circuit

21 CFR 868.5260 / Anesthesiology

CAH is the FDA product code for Filter, Bacterial, Breathing-Circuit, a class II device type, regulated under 21 CFR 868.5260. As of 2026-09-10, FDA records hold 202 510(k) clearances under this code, the most recent dated 2026-05-15, and 28 recalls.

Classification record

Product code: CAH
Device name: Filter, Bacterial, Breathing-Circuit
Regulation: 21 CFR 868.5260
Device class: Class II
Review panel: Anesthesiology
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 202
Ingested recalls: 28

Clearances, product code CAH

By decision year

202 clearances under product code CAH with a decision year between 1976 and 2026, 1993 the highest year at 12.

Show the numbers

510(k) clearances under FDA product code CAH by decision year
Year	Clearances
1976	4
1977	5
1978	2
1979	4
1980	4
1981	4
1982	4
1983	6
1984	7
1985	4
1986	5
1987	2
1988	4
1989	9
1990	5
1991	4
1992	4
1993	12
1994	9
1995	7
1996	6
1997	7
1998	6
1999	3
2000	2
2001	7
2002	9
2003	5
2004	5
2005	4
2006	1
2007	2
2008	1
2009	4
2010	5
2011	3
2012	3
2013	1
2014	4
2015	2
2017	1
2019	2
2020	2
2021	2
2022	3
2023	3
2024	2
2026	2

Applicants with the most clearances

Product code CAH

Applicants holding the most 510(k) clearances under product code CAH
Applicant	Clearances
Intersurgical Ltd.	10
Medipart Jerry Alexander	8
Pentair Filtration Solutions	6
GE Healthcare	5
King Systems Corporation.	5
Mallinckrodt Medical	5
Omnicon Medical Corp.	5
Vital Signs, Inc.	5
Arc Medical, Inc.	4
Marquest Medical Products, Inc.	4

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 127 companies shown, in name order