Avl Model 940 Automatic Ph/Blood Gas

FDA 510(k) K792230 · Gauntlet Technology Corp.

Substantially Equivalent

510(k) numberK792230

Submission

Device name
Avl Model 940 Automatic Ph/Blood Gas
Applicant
Gauntlet Technology Corp.
Mchenry, IL, US
Received
November 5, 1979
Decision date
December 31, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CHL – Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1120
Specialty
Clinical Chemistry

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Questions and answers

When was Avl Model 940 Automatic Ph/Blood Gas cleared by the FDA?

Avl Model 940 Automatic Ph/Blood Gas (K792230) received a 510(k) decision of Substantially Equivalent on December 31, 1979, 56 days after the submission was received.

What is the product code of K792230?

The FDA product code is CHL – Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph, a Class II (moderate risk) device regulated under 21 CFR 862.1120.