NGDClass I

Test, Lactic Acid, Over The Counter

21 CFR 862.1450 / Clinical Chemistry

NGD is the FDA product code for Test, Lactic Acid, Over The Counter, a class I device type, regulated under 21 CFR 862.1450. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: NGD
Device name: Test, Lactic Acid, Over The Counter
Regulation: 21 CFR 862.1450
Device class: Class I
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

Nova Biomedical Corporation

Recent clearances

Product code NGD

FDA records hold no clearances under product code NGD.

Recent recalls

Product code NGD

FDA records show no recalls under product code NGD.

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)