BYXClass I

Tubing, Pressure And Accessories

21 CFR 868.5860 / Anesthesiology

BYX is the FDA product code for Tubing, Pressure And Accessories, a class I device type, regulated under 21 CFR 868.5860. As of 2026-09-10, FDA records hold 62 510(k) clearances under this code, the most recent dated 2001-06-13, and one recall.

Classification record

Product code: BYX
Device name: Tubing, Pressure And Accessories
Regulation: 21 CFR 868.5860
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: 62
Ingested recalls: 1

Clearances, product code BYX

By decision year

62 clearances under product code BYX with a decision year between 1976 and 2001, 1981 the highest year at 10.

Show the numbers

510(k) clearances under FDA product code BYX by decision year
Year	Clearances
1976	1
1977	1
1978	3
1979	9
1980	8
1981	10
1982	2
1983	4
1984	2
1985	3
1986	2
1990	7
1991	2
1992	2
1993	2
1994	2
1996	1
2001	1

Applicants with the most clearances

Product code BYX

Applicants holding the most 510(k) clearances under product code BYX
Applicant	Clearances
Medical Fittings, Inc.	12
Airlife, Inc.	7
Timeter Instrument Corp.	5
Mem Medical, Inc.	3
Todd Industries, Inc.	3
Chad Therapeutics, Inc.	2
Intec Medical, Inc.	2
Medi-Craft, Ltd.	2
Seven Harvest Intl. Import & Export	2
Auburn Components	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 210 companies shown, in name order