510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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JZQClass I

Plates And Equipment, Radial Immunodiffusion

21 CFR 866.4800 / Immunology
FDA source (opens on fda.gov)

JZQ is the FDA product code for Plates And Equipment, Radial Immunodiffusion, a class I device type, regulated under 21 CFR 866.4800. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
JZQ
Device name
Plates And Equipment, Radial Immunodiffusion
Regulation
21 CFR 866.4800
Device class
Class I
Review panel
Immunology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
7
Ingested recalls
1

Clearances, product code JZQ

By decision year
7 clearances under product code JZQ with a decision year between 1976 and 1988, 1988 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JZQ by decision year
YearClearances
19761
19771
19791
19801
19831
19882

Applicants with the most clearances

Product code JZQ
Applicants holding the most 510(k) clearances under product code JZQ
ApplicantClearances
Calbiochem-Behring Corp.1
Dynatech Laboratories, Inc.1
Helena Laboratories, Corp.1
Hyland Therapeutic Div., Travenol Laboratories1
Meridian Diagnostics, Inc.1
Miles Laboratories, Inc.1
The Binding Site1

Companies listing this code with FDA

Companies whose registered establishments list this code