510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K843938Substantially Equivalent

Linear Enzymatic Uric Acid System

Simmler Inc, St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K843938 is the FDA 510(k) clearance record for LINEAR ENZYMATIC URIC ACID SYSTEM, a class I device, cleared for Simmler, Inc. on under FDA product code KNK (Acid, Uric, Uricase (Colorimetric)). FDA records list 23 510(k) clearances for Simmler, Inc., from to . As of , FDA records show no recalls naming K843938.

Clearance record

Decision date
Received
(21 days to decision)
Product code
KNK Acid, Uric, Uricase (Colorimetric)
Regulation
21 CFR 862.1775
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Simmler, Inc. 3755 Forest Park Ave., St. Louis MO
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