DSAClass II

Cable, Transducer And Electrode, Patient, (Including Connector)

21 CFR 870.2900 / Cardiovascular

DSA is the FDA product code for Cable, Transducer And Electrode, Patient, (Including Connector), a class II device type, regulated under 21 CFR 870.2900. As of 2026-09-10, FDA records hold 105 510(k) clearances under this code, the most recent dated 2026-01-18, and 12 recalls.

Classification record

Product code: DSA
Device name: Cable, Transducer And Electrode, Patient, (Including Connector)
Regulation: 21 CFR 870.2900
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: 105
Ingested recalls: 12

Clearances, product code DSA

By decision year

105 clearances under product code DSA with a decision year between 1977 and 2026, 1994 the highest year at 8.

Show the numbers

510(k) clearances under FDA product code DSA by decision year
Year	Clearances
1977	4
1980	6
1982	1
1987	1
1988	3
1989	4
1990	1
1991	1
1992	1
1993	2
1994	8
1995	1
1996	3
1997	1
1998	3
1999	1
2000	3
2001	2
2002	3
2003	1
2005	1
2006	1
2007	2
2008	6
2010	4
2011	1
2012	1
2013	1
2014	1
2016	2
2017	5
2018	3
2019	4
2020	6
2021	4
2022	2
2023	3
2024	3
2025	4
2026	1

Applicants with the most clearances

Product code DSA

Applicants holding the most 510(k) clearances under product code DSA
Applicant	Clearances
Medtronic, Inc.	7
Tronomed, Inc.	4
Arbo Medical, Inc.	3
Jaeger Medical GmbH	3
Baylis Medical Technologies Inc.	2
Beijing Rongrui-Century Science & Technology Co., Ltd.	2
Boston Scientific Corporation	2
C.R. Bard Inc	2
Conmedcorp	2
Curbell Electronics, Inc.	2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 108 companies shown, in name order