Avl Opti Critical Care Analyzer

FDA 510(k) K974784 · Avl Scientific Corp.

Substantially Equivalent

510(k) numberK974784

Submission

Device name
Avl Opti Critical Care Analyzer
Applicant
Avl Scientific Corp.
Roswell, GA, US
Received
December 22, 1997
Decision date
February 24, 1998
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 Avl Opti Critical Care Analyzer cleared by the FDA?

Avl Opti Critical Care Analyzer (K974784) received a 510(k) decision of Substantially Equivalent on February 24, 1998, 64 days after the submission was received.

What is the product code of K974784?

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