510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K843758Substantially Equivalent

Uropaper Eiken Gk

Syn-Kit, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K843758 is the FDA 510(k) clearance record for UROPAPER EIKEN GK, a class II device, cleared for Syn-Kit, Inc. on under FDA product code JIL (Method, Enzymatic, Glucose (Urinary, Non-Quantitative)). FDA records list 34 510(k) clearances for Syn-Kit, Inc., from to . As of , FDA records show no recalls naming K843758.

Clearance record

Decision date
Received
(84 days to decision)
Product code
JIL Method, Enzymatic, Glucose (Urinary, Non-Quantitative)
Regulation
21 CFR 862.1340
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Syn-Kit, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code JIL

Trailing 12 months

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

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