510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K113726Substantially Equivalent

Epoc Chloride Test and Epoc Creatinine Test

Epocal Inc, Ottawa, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K113726 is the FDA 510(k) clearance record for EPOC CHLORIDE TEST AND EPOC CREATININE TEST, a class II device, cleared for Epocal, Inc. on under FDA product code CGL (Electrode, Ion Based, Enzymatic, Creatinine). FDA records list 7 510(k) clearances for Epocal, Inc., from to . As of , FDA records show no recalls naming K113726.

Clearance record

Decision date
Received
(291 days to decision)
Product code
CGL Electrode, Ion Based, Enzymatic, Creatinine
Regulation
21 CFR 862.1225
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Epocal, Inc. 2060 Walkley Rd., Ottawa, CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CGL

Trailing 12 months
1 clearance under product code CGL in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CGL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260