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

Tetrabromophenolphthalein, Albumin

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

CJF is the FDA product code for Tetrabromophenolphthalein, 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
CJF
Device name
Tetrabromophenolphthalein, 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 CJF

By decision year
1 clearance under product code CJF with a decision year between 1983 and 1983, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CJF by decision year
YearClearances
19831

Applicants with the most clearances

Product code CJF
Applicants holding the most 510(k) clearances under product code CJF
ApplicantClearances
Amresco, 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 CJF.