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

Jenner Stain

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

KJX is the FDA product code for Jenner Stain, 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
KJX
Device name
Jenner Stain
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 KJX

By decision year
1 clearance under product code KJX with a decision year between 1984 and 1984, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KJX by decision year
YearClearances
19841

Applicants with the most clearances

Product code KJX
Applicants holding the most 510(k) clearances under product code KJX
ApplicantClearances
E K Ind., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code