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

Carbol Night Blue

21 CFR 864.1850 / Hematology
FDA source (opens on fda.gov)

ICJ is the FDA product code for Carbol Night Blue, a class I device type, regulated under 21 CFR 864.1850. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
ICJ
Device name
Carbol Night Blue
Regulation
21 CFR 864.1850
Device class
Class I
Review panel
Hematology
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 ICJ

By decision year
1 clearance under product code ICJ with a decision year between 1987 and 1987, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code ICJ by decision year
YearClearances
19871

Applicants with the most clearances

Product code ICJ
Applicants holding the most 510(k) clearances under product code ICJ
ApplicantClearances
BD Becton Dickinson Vacutainer Systems Preanalytic1

Companies listing this code with FDA

Companies whose registered establishments list this code

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