LFQ — Acid, Uric, Acid Reduction Of Ferric Ion Class I

FDA Device Classification

FDA product code LFQ covers "Acid, Uric, Acid Reduction Of Ferric Ion", a Class I medical device regulated under 21 CFR 862.1775. Submissions are reviewed by the Clinical Chemistry panel. At least 5 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LFQ
Device Class
Class I
Regulation Number
862.1775
Submission Type
Review Panel
CH
Medical Specialty
Clinical Chemistry
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K860111technostics intlURIC ACID REAGENT SETFebruary 19, 1986
K860142sterling diagnosticsURIC ACID REAGENT SET (COLORIMETRIC)February 11, 1986
K844075livonia diagnosticsURIC ACID REAGENT SETOctober 30, 1984
K812313sandare chemical coSANDARE URIC ACID PROCEDURESeptember 1, 1981
K811764anco medical reagents and assocURIC ACID REAGENT SETAugust 20, 1981