QLHNot classified

System, Intravaginal, For Controlled Release Of Drug Substance, Cder Or Cber Led

Unknown

QLH is the FDA product code for System, Intravaginal, For Controlled Release Of Drug Substance, Cder Or Cber Led. FDA's definition for this code reads: "Intravaginal systems for controlled release of drug substance are products that are inserted into the vagina and provide controlled release of drug products". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: QLH
Device name: System, Intravaginal, For Controlled Release Of Drug Substance, Cder Or Cber Led
FDA definition: Intravaginal systems for controlled release of drug substance are products that are inserted into the vagina and provide controlled release of drug products
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 QLH.

Recent clearances

Product code QLH

FDA records hold no clearances under product code QLH.

Recent recalls

Product code QLH

FDA records show no recalls under product code QLH.

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)