EasyStat 300

FDA 510(k) K220396 · Medica Corporation

Substantially Equivalent

510(k) numberK220396

Submission

Device name
EasyStat 300
Applicant
Medica Corporation
Bedford, MA, US
Received
February 11, 2022
Decision date
September 26, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CEM – Electrode, Ion Specific, Potassium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1600
Specialty
Clinical Chemistry

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Questions and answers

When was EasyStat 300 cleared by the FDA?

EasyStat 300 (K220396) received a 510(k) decision of Substantially Equivalent on September 26, 2023, 592 days after the submission was received.

What is the product code of K220396?

The FDA product code is CEM – Electrode, Ion Specific, Potassium, a Class II (moderate risk) device regulated under 21 CFR 862.1600.