QIXNot classified

System, Transdermal Delivery, Cder Or Cber Led

Unknown

QIX is the FDA product code for System, Transdermal Delivery, Cder Or Cber Led. FDA's definition for this code reads: "Drug delivery systems designed to deliver at least one therapeutically active ingredient (drug substance) across the skin for systemic effect". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: QIX
Device name: System, Transdermal Delivery, Cder Or Cber Led
FDA definition: Drug delivery systems designed to deliver at least one therapeutically active ingredient (drug substance) across the skin for systemic effect.
Device class: Not classified
Review panel: Unknown
Submission type: Contact ODE
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

No registered establishment in MDM’s records lists product code QIX.

Recent clearances

Product code QIX

FDA records hold no clearances under product code QIX.

Recent recalls

Product code QIX

FDA records show no recalls under product code QIX.

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)