URIC ACID REAGENT SET— 510(k) K811764

Name: FDA 510(k) clearance K811764
Creator: U.S. Food and Drug Administration
Published: 1981-08-20

Substantially Equivalent

Anco Medical Reagents & Assoc.

FDA 510(k) clearance K811764 for URIC ACID REAGENT SET, Substantially Equivalent on 1981-08-20. Applicant: Anco Medical Reagents & Assoc.. Device class: 1.

Clearance details

Applicant: Anco Medical Reagents & Assoc.
Product code: Code LFQ
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1981-06-22
Decision date: 1981-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LFQ

view all

K860111 — URIC ACID REAGENT SET1986-02-19
K860142 — URIC ACID REAGENT SET (COLORIMETRIC)1986-02-11
K844075 — URIC ACID REAGENT SET1984-10-30
K812313 — SANDARE URIC ACID PROCEDURE1981-09-01

More clearances from Anco Medical Reagents & Assoc.

view all

K842440 — SICKLE CELL STAT A/S HETEROZYGOUS-ERYTH1984-07-27
K831871 — SICKLE-HEME A/S CONTROLS & A/A CONTROL1983-07-28
K821658 — HEMOGLOBIN REAGENT1982-06-25
K821526 — ACID PHOSPHATASE REAGENT SET1982-06-10
K821102 — MEGNESIUM REAGENT KIT1982-05-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.