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

Media, Mounting, Water Soluble

21 CFR 864.4010 / Pathology
FDA source (opens on fda.gov)

KEQ is the FDA product code for Media, Mounting, Water Soluble, a class I device type, regulated under 21 CFR 864.4010. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KEQ
Device name
Media, Mounting, Water 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
7
Ingested recalls
0

Clearances, product code KEQ

By decision year
7 clearances under product code KEQ with a decision year between 1978 and 1983, 1978 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code KEQ by decision year
YearClearances
19783
19803
19831

Applicants with the most clearances

Product code KEQ
Applicants holding the most 510(k) clearances under product code KEQ
ApplicantClearances
Meridian Diagnostics, Inc.3
Marion Laboratories, Inc.2
Flow Laboratories, Inc.1
Surgipath Medical Industries, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code