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

Tetrabromo-M-Cresolsulfonphthalein, Albumin

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

CJG is the FDA product code for Tetrabromo-M-Cresolsulfonphthalein, 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
CJG
Device name
Tetrabromo-M-Cresolsulfonphthalein, 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 CJG

By decision year
1 clearance under product code CJG with a decision year between 1997 and 1997, 1997 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code CJG by decision year
YearClearances
19971

Applicants with the most clearances

Product code CJG
Applicants holding the most 510(k) clearances under product code CJG
ApplicantClearances
Bayer Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code