KZDClass I

Infusor, Pressure, For I.V. Bags

21 CFR 880.5420 / General Hospital

KZD is the FDA product code for Infusor, Pressure, For I.V. Bags, a class I device type, regulated under 21 CFR 880.5420. As of 2026-09-10, FDA records hold 35 510(k) clearances under this code, the most recent dated 1998-02-17, and 14 recalls.

Classification record

Product code: KZD
Device name: Infusor, Pressure, For I.V. Bags
Regulation: 21 CFR 880.5420
Device class: Class I
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: 35
Ingested recalls: 14

Clearances, product code KZD

By decision year

35 clearances under product code KZD with a decision year between 1976 and 1998, 1976 the highest year at 4.

Show the numbers

510(k) clearances under FDA product code KZD by decision year
Year	Clearances
1976	4
1977	2
1978	2
1980	1
1981	2
1982	3
1983	1
1985	1
1986	4
1987	1
1988	1
1989	1
1990	2
1991	2
1992	1
1993	2
1994	1
1995	2
1997	1
1998	1

Applicants with the most clearances

Product code KZD

Applicants holding the most 510(k) clearances under product code KZD
Applicant	Clearances
Biomedical Dynamics, Inc.	3
Tecnadyne Scientific, Inc.	2
Travenol Laboratories, S.A.	2
Abbott Medical	1
Allen Medical Systems, Inc.	1
Bio-Medical Instruments, Ltd.	1
Calbio, Inc.	1
Circulatory Technology, Inc.	1
Crest Medical Equipment	1
Datascope Corp.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 74 companies shown, in name order