DKSClass I

Plate, Silica Gel, Tlc

21 CFR 862.2270 / Clinical Chemistry

DKS is the FDA product code for Plate, Silica Gel, Tlc, a class I device type, regulated under 21 CFR 862.2270. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: DKS
Device name: Plate, Silica Gel, Tlc
Regulation: 21 CFR 862.2270
Device class: Class I
Review panel: Clinical Chemistry
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

Scantibodies Laboratory Inc.

Recent clearances

Product code DKS

FDA records hold no clearances under product code DKS.

Recent recalls

Product code DKS

FDA records show no recalls under product code DKS.

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)