DXCClass II

Clamp, Vascular

21 CFR 870.4450 / Cardiovascular

DXC is the FDA product code for Clamp, Vascular, a class II device type, regulated under 21 CFR 870.4450. As of 2026-09-10, FDA records hold 205 510(k) clearances under this code, the most recent dated 2026-07-22, and 26 recalls.

Classification record

Product code: DXC
Device name: Clamp, Vascular
Regulation: 21 CFR 870.4450
Device class: Class II
Review panel: Cardiovascular
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 205
Ingested recalls: 26

Clearances, product code DXC

By decision year

205 clearances under product code DXC with a decision year between 1976 and 2026, 2013 the highest year at 14.

Show the numbers

510(k) clearances under FDA product code DXC by decision year
Year	Clearances
1976	1
1977	2
1979	1
1980	2
1981	3
1982	1
1983	1
1984	1
1985	2
1986	2
1988	7
1989	4
1990	3
1991	2
1992	4
1993	2
1994	2
1995	6
1996	10
1997	11
1998	11
1999	8
2000	5
2001	4
2002	11
2003	3
2004	5
2005	1
2006	6
2007	10
2008	3
2009	4
2010	2
2011	6
2012	5
2013	14
2014	4
2015	5
2016	3
2017	3
2018	2
2019	2
2020	3
2021	6
2022	1
2023	4
2024	1
2025	2
2026	4

Applicants with the most clearances

Product code DXC

Applicants holding the most 510(k) clearances under product code DXC
Applicant	Clearances
Radi Medical Systems AB	8
Cardiva Medical, Inc.	7
Advanced Vascular Dynamics	6
Novare Surgical Systems, Inc.	6
Medtronic, Inc.	5
Applied Vascular Devices, Inc.	5
Edwards Lifesciences LLC	5
Heartport, Inc.	5
Innovative Trauma Care Inc	4
Rmds, Inc.	4

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 152 companies shown, in name order