KEPClass I

Media, Mounting, Oil Soluble

21 CFR 864.4010 / Pathology

KEP is the FDA product code for Media, Mounting, Oil Soluble, a class I device type, regulated under 21 CFR 864.4010. As of 2026-09-10, FDA records hold 3 510(k) clearances under this code, the most recent dated 1983-03-17, and no recalls.

Classification record

Product code: KEP
Device name: Media, Mounting, Oil Soluble
Regulation: 21 CFR 864.4010
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: 3
Ingested recalls: 0

Clearances, product code KEP

By decision year

3 clearances under product code KEP with a decision year between 1980 and 1983, 1980 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code KEP by decision year
Year	Clearances
1980	1
1981	1
1983	1

Applicants with the most clearances

Product code KEP

Applicants holding the most 510(k) clearances under product code KEP
Applicant	Clearances
Mcb Manufacturing Chemists, Inc.	1
Surgipath	1
Surgipath Medical Industries, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code KEP

Recent recalls

Product code KEP

FDA records show no recalls under product code KEP.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)