LHPClass III

System, Telethermographic (Sole Diagnostic Screen)

21 CFR 884.2980 / Obstetrics/Gynecology

LHP is the FDA product code for System, Telethermographic (Sole Diagnostic Screen), a class III device type, regulated under 21 CFR 884.2980. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: LHP
Device name: System, Telethermographic (Sole Diagnostic Screen)
Regulation: 21 CFR 884.2980
Device class: Class III
Review panel: Obstetrics/Gynecology
Submission type: PMA
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 LHP.

Recent clearances

Product code LHP

FDA records hold no clearances under product code LHP.

Recent recalls

Product code LHP

FDA records show no recalls under product code LHP.

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)