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

Radial Immunodiffusion, Albumin

21 CFR 862.1035 / Clinical Chemistry
FDA source (opens on fda.gov)

CJQ is the FDA product code for Radial Immunodiffusion, Albumin, a class II device type, regulated under 21 CFR 862.1035. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
CJQ
Device name
Radial Immunodiffusion, Albumin
Regulation
21 CFR 862.1035
Device class
Class II
Review panel
Clinical Chemistry
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code CJQ

By decision year
1 clearance under product code CJQ with a decision year between 1981 and 1981, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CJQ by decision year
YearClearances
19811

Applicants with the most clearances

Product code CJQ
Applicants holding the most 510(k) clearances under product code CJQ
ApplicantClearances
Meloy Laboratories, 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 CJQ.