KDQClass II

Bottle, Collection, Vacuum

21 CFR 880.6740 / General Hospital

KDQ is the FDA product code for Bottle, Collection, Vacuum, a class II device type, regulated under 21 CFR 880.6740. As of 2026-09-10, FDA records hold 48 510(k) clearances under this code, the most recent dated 2008-07-25, and 33 recalls.

Classification record

Product code: KDQ
Device name: Bottle, Collection, Vacuum
Regulation: 21 CFR 880.6740
Device class: Class II
Review panel: General Hospital
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 48
Ingested recalls: 33

Clearances, product code KDQ

By decision year

48 clearances under product code KDQ with a decision year between 1976 and 2008, 1981 the highest year at 8.

Show the numbers

510(k) clearances under FDA product code KDQ by decision year
Year	Clearances
1976	1
1977	1
1978	2
1979	2
1980	3
1981	8
1983	1
1985	6
1986	5
1988	3
1989	1
1990	3
1991	2
1993	1
1994	1
1995	1
1996	3
1999	1
2005	1
2006	1
2008	1

Applicants with the most clearances

Product code KDQ

Applicants holding the most 510(k) clearances under product code KDQ
Applicant	Clearances
Atrium Medical Corporation	8
Deknatel, Inc.	5
Abco Dealers, Inc.	2
BD Becton Dickinson Vacutainer Systems Preanalytic	2
Boehringer Laboratories, LLC	2
Davol, Inc.	2
Sherwood Medical Co.	2
Anchor Brush Co., Inc.	1
Apex Medical, Inc.	1
Bentley Laboratories, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 246 companies shown, in name order