LFSClass II

Radioreceptor Assay, Human Chorionic Gonadotropin

21 CFR 862.1155 / Clinical Chemistry

LFS is the FDA product code for Radioreceptor Assay, Human Chorionic Gonadotropin, a class II device type, regulated under 21 CFR 862.1155. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: LFS
Device name: Radioreceptor Assay, Human Chorionic Gonadotropin
Regulation: 21 CFR 862.1155
Device class: Class II
Review panel: Clinical Chemistry
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
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 LFS.

Recent clearances

Product code LFS

FDA records hold no clearances under product code LFS.

Recent recalls

Product code LFS

FDA records show no recalls under product code LFS.

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)