JQWClass I

Station, Pipetting And Diluting, For Clinical Use

21 CFR 862.2750 / Clinical Chemistry

JQW is the FDA product code for Station, Pipetting And Diluting, For Clinical Use, a class I device type, regulated under 21 CFR 862.2750. As of 2026-09-10, FDA records hold 140 510(k) clearances under this code, the most recent dated 2003-06-24, and 36 recalls.

Classification record

Product code: JQW
Device name: Station, Pipetting And Diluting, For Clinical Use
Regulation: 21 CFR 862.2750
Device class: Class I
Review panel: Clinical Chemistry
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 140
Ingested recalls: 36

Clearances, product code JQW

By decision year

140 clearances under product code JQW with a decision year between 1977 and 2003, 1984 the highest year at 12.

Show the numbers

510(k) clearances under FDA product code JQW by decision year
Year	Clearances
1977	9
1978	8
1979	3
1980	10
1981	7
1982	6
1983	8
1984	12
1985	5
1986	8
1987	6
1988	3
1989	12
1990	6
1991	6
1992	9
1993	1
1994	9
1995	3
1996	3
1997	3
1998	2
2003	1

Applicants with the most clearances

Product code JQW

Applicants holding the most 510(k) clearances under product code JQW
Applicant	Clearances
Denley Instruments, Inc.	8
Dynatech Laboratories, Inc.	7
Tecan U.S.	7
Hamilton Co	6
Micromedic Systems	6
Siemens Healthcare Diagnostics Inc.	5
Syva Co.	4
Abbott Medical	3
American Dade	3
Beckman Instruments, Inc.	3

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 65 companies shown, in name order