510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K092849Substantially Equivalent

Blood Collection Tube Samples for Use with Point of Care Blood Analyzer

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

K092849 is the FDA 510(k) clearance record for BLOOD COLLECTION TUBE SAMPLES FOR USE WITH POINT OF CARE BLOOD ANALYZER, a class II device, cleared for Epocal, Inc. on under FDA product code CEM (Electrode, Ion Specific, Potassium). FDA records list 7 510(k) clearances for Epocal, Inc., from to . As of , FDA records show no recalls naming K092849.

Clearance record

Decision date
Received
(195 days to decision)
Product code
CEM Electrode, Ion Specific, Potassium
Regulation
21 CFR 862.1600
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 CEM

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