510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811764Substantially Equivalent

Uric Acid Reagent Set

Anco Medical Reagents & Assoc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811764 is the FDA 510(k) clearance record for URIC ACID REAGENT SET, a class I device, cleared for Anco Medical Reagents & Assoc. on under FDA product code LFQ (Acid, Uric, Acid Reduction Of Ferric Ion). FDA records list 26 510(k) clearances for Anco Medical Reagents & Assoc., from to . As of , FDA records show no recalls naming K811764.

Clearance record

Decision date
Received
(59 days to decision)
Product code
LFQ Acid, Uric, Acid Reduction Of Ferric Ion
Regulation
21 CFR 862.1775
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Anco Medical Reagents & Assoc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LFQ

Trailing 12 months

FDA records hold no clearances under product code LFQ in the trailing twelve months.

FDA records show no clearances under product code LFQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LFQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260