Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K811810Substantially Equivalent

Uric Acid Test

Environmental Chemical Specialties, Mchenry IL / Traditional, Substantially Equivalent

K811810 is the FDA 510(k) clearance record for URIC ACID TEST, a class I device, cleared for Environmental Chemical Specialties on under FDA product code KNK (Acid, Uric, Uricase (Colorimetric)). FDA records list 15 510(k) clearances for Environmental Chemical Specialties, from to . As of , FDA records show no recalls naming K811810.

Clearance record

Decision date
Received
(20 days to decision)
Product code
KNK Acid, Uric, Uricase (Colorimetric)
Regulation
21 CFR 862.1775
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Environmental Chemical Specialties 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KNK

Trailing 12 months

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

FDA records show no clearances under product code KNK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KNK, 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