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

Brilliant Cresyl Blue

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

KJN is the FDA product code for Brilliant Cresyl 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
KJN
Device name
Brilliant Cresyl 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 KJN

By decision year
1 clearance under product code KJN with a decision year between 1982 and 1982, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KJN by decision year
YearClearances
19821

Applicants with the most clearances

Product code KJN
Applicants holding the most 510(k) clearances under product code KJN
ApplicantClearances
R & D Systems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code