Carbon Dioxide Analyzer

FDA 510(k) K771610 · Corning Medical & Scientific

Substantially Equivalent

510(k) numberK771610

Submission

Device name
Carbon Dioxide Analyzer
Applicant
Corning Medical & Scientific
Mchenry, IL, US
Received
August 22, 1977
Decision date
October 7, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CIE – Volumetric/Manometric, Carbon-Dioxide
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1160
Specialty
Clinical Chemistry

Other 510(k)s with product code CIE

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K904761P/N 35310, Il Test Alkaline Phosphatase ReagentCIE · Traditional Instrumentation Laboratory CO11/20/1990SE
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K820091Airmed Smoke Evacuation & FilterCIE · Traditional James L. Geraci & Associates, Inc.02/24/1982SE
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Questions and answers

When was Carbon Dioxide Analyzer cleared by the FDA?

Carbon Dioxide Analyzer (K771610) received a 510(k) decision of Substantially Equivalent on October 7, 1977, 46 days after the submission was received.

What is the product code of K771610?

The FDA product code is CIE – Volumetric/Manometric, Carbon-Dioxide, a Class II (moderate risk) device regulated under 21 CFR 862.1160.