DQYClass II

Catheter, Percutaneous

21 CFR 870.1250 / Cardiovascular

DQY is the FDA product code for Catheter, Percutaneous, a class II device type, regulated under 21 CFR 870.1250. As of 2026-09-10, FDA records hold 895 510(k) clearances under this code, the most recent dated 2026-08-14, and 620 recalls.

Classification record

Product code: DQY
Device name: Catheter, Percutaneous
Regulation: 21 CFR 870.1250
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: 896
Ingested recalls: 620

Clearances, product code DQY

By decision year

896 clearances under product code DQY with a decision year between 1979 and 2026, 2009 the highest year at 37.

Show the numbers

510(k) clearances under FDA product code DQY by decision year
Year	Clearances
1979	1
1980	1
1981	5
1982	7
1983	10
1984	19
1985	13
1986	17
1987	19
1988	12
1989	10
1990	13
1991	23
1992	8
1993	11
1994	18
1995	20
1996	5
1997	11
1998	10
1999	11
2000	9
2001	28
2002	32
2003	31
2004	25
2005	25
2006	27
2007	16
2008	31
2009	37
2010	22
2011	36
2012	30
2013	32
2014	19
2015	27
2016	22
2017	26
2018	25
2019	30
2020	20
2021	18
2022	18
2023	18
2024	16
2025	21
2026	11

Applicants with the most clearances

Product code DQY

Applicants holding the most 510(k) clearances under product code DQY
Applicant	Clearances
Boston Scientific Corporation	61
Medtronic, Inc.	50
Abbott Medical	37
Vascular Solutions LLC	27
BIOTRONIK AG	23
Cordis US Corp.	23
Advanced Cardiovascular Systems, Inc.	19
Asahi Intecc Co., Ltd.	19
Concentric Medical, Inc.	19
Cook Inc.	18

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 209 companies shown, in name order