CANClass I

Regulator, Pressure, Gas Cylinder

21 CFR 868.2700 / Anesthesiology

CAN is the FDA product code for Regulator, Pressure, Gas Cylinder, a class I device type, regulated under 21 CFR 868.2700. As of 2026-09-10, FDA records hold 55 510(k) clearances under this code, the most recent dated 2017-03-02, and 17 recalls.

Classification record

Product code: CAN
Device name: Regulator, Pressure, Gas Cylinder
Regulation: 21 CFR 868.2700
Device class: Class I
Review panel: Anesthesiology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 55
Ingested recalls: 17

Clearances, product code CAN

By decision year

55 clearances under product code CAN with a decision year between 1977 and 2017, 1985 the highest year at 6.

Show the numbers

510(k) clearances under FDA product code CAN by decision year
Year	Clearances
1977	1
1978	5
1980	1
1981	4
1982	2
1983	1
1984	3
1985	6
1986	4
1987	3
1988	1
1989	5
1990	6
1991	1
1992	4
1993	1
1994	1
1995	2
2006	2
2009	1
2017	1

Applicants with the most clearances

Product code CAN

Applicants holding the most 510(k) clearances under product code CAN
Applicant	Clearances
Medtronic, Inc.	3
Airco, Inc.	2
C.G.H. Medical, Inc.	2
Instrumentation Industries, Incorporated	2
Lifeguard Medical Products, Inc.	2
Modern Engineering Co., Inc.	2
Precision Medical, Inc.	2
Safety Laboratories West	2
Salter Labs	2
Thermadyne Holings Corp.	2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 107 companies shown, in name order