JQQClass I

Dialyzer

21 CFR 862.2050 / Clinical Chemistry

JQQ is the FDA product code for Dialyzer, a class I device type, regulated under 21 CFR 862.2050. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1976-12-06, and no recalls.

Classification record

Product code: JQQ
Device name: Dialyzer
Regulation: 21 CFR 862.2050
Device class: Class I
Review panel: Clinical Chemistry
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: Yes
Third party review eligible: No
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code JQQ

By decision year

1 clearance under product code JQQ with a decision year between 1976 and 1976, 1976 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code JQQ by decision year
Year	Clearances
1976	1

Applicants with the most clearances

Product code JQQ

Applicants holding the most 510(k) clearances under product code JQQ
Applicant	Clearances
Amicon, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code JQQ.

Recent clearances

Product code JQQ

K761100Class IMulti-Cell Ultrafiltration SystemAmicon, Inc. / cleared 1976-12-06

Recent recalls

Product code JQQ

FDA records show no recalls under product code JQQ.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)