CADClass II

Vaporizer, Anesthesia, Non-Heated

21 CFR 868.5880 / Anesthesiology

CAD is the FDA product code for Vaporizer, Anesthesia, Non-Heated, a class II device type, regulated under 21 CFR 868.5880. As of 2026-09-10, FDA records hold 57 510(k) clearances under this code, the most recent dated 2024-10-31, and 13 recalls.

Classification record

Product code: CAD
Device name: Vaporizer, Anesthesia, Non-Heated
Regulation: 21 CFR 868.5880
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: 57
Ingested recalls: 13

Clearances, product code CAD

By decision year

57 clearances under product code CAD with a decision year between 1976 and 2024, 1995 the highest year at 5.

Show the numbers

510(k) clearances under FDA product code CAD by decision year
Year	Clearances
1976	2
1977	3
1978	1
1979	1
1981	1
1982	2
1983	1
1984	2
1985	1
1986	3
1987	2
1988	1
1989	3
1992	1
1993	1
1994	1
1995	5
1996	5
1997	2
1998	4
1999	1
2000	2
2001	1
2002	1
2003	1
2004	2
2005	1
2006	2
2011	1
2015	1
2018	1
2024	1

Applicants with the most clearances

Product code CAD

Applicants holding the most 510(k) clearances under product code CAD
Applicant	Clearances
GE Healthcare	9
Penlon, Ltd.	9
Draeger, Inc.	7
Southmedic Inc.	5
Ohio Medical Products	2
Shenzhen Mindray Bio-Medical Electronics Co.,LTD	2
Technimeca Medic, Inc.	2
Air Products & Chemicals, Inc.	1
Anesthetic Vaporizer Services	1
Bear Medical Systems, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code