QGUClass II

Hemoglobin For Donor Testing

21 CFR 864.7500 / Hematology

QGU is the FDA product code for Hemoglobin For Donor Testing, a class II device type, regulated under 21 CFR 864.7500. FDA's definition for this code reads: "Assays hemoglobin concentration test for blood donors". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: QGU
Device name: Hemoglobin For Donor Testing
FDA definition: Assays hemoglobin concentration test for blood donors.
Regulation: 21 CFR 864.7500
Device class: Class II
Review panel: Hematology
Submission type: 510(k)
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

Orsense Ltd

Recent clearances

Product code QGU

FDA records hold no clearances under product code QGU.

Recent recalls

Product code QGU

FDA records show no recalls under product code QGU.

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)