Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K090109Substantially Equivalent

Blood Gas, Electrolyte and Metabolite Test Card

Epocal Inc, Ottawa, CA / Traditional, Substantially Equivalent

K090109 is the FDA 510(k) clearance record for BLOOD GAS, ELECTROLYTE AND METABOLITE TEST CARD, a class II device, cleared for Epocal, Inc. on under FDA product code CGA (Glucose Oxidase, Glucose). FDA records list 7 510(k) clearances for Epocal, Inc., from to . As of , FDA records show 3 recalls naming K090109.

Clearance record

Decision date
Received
(160 days to decision)
Product code
CGA Glucose Oxidase, Glucose
Regulation
21 CFR 862.1345
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 CGA

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