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

Stages, Microscope

21 CFR 864.3600 / Pathology
FDA source (opens on fda.gov)

KEJ is the FDA product code for Stages, Microscope, a class I device type, regulated under 21 CFR 864.3600. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KEJ
Device name
Stages, Microscope
Regulation
21 CFR 864.3600
Device class
Class I
Review panel
Pathology
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 KEJ

By decision year
1 clearance under product code KEJ with a decision year between 1988 and 1988, 1988 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KEJ by decision year
YearClearances
19881

Applicants with the most clearances

Product code KEJ
Applicants holding the most 510(k) clearances under product code KEJ
ApplicantClearances
Cryodyne Technologies, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code