Multecon Blood Gas Control

FDA 510(k) K790813 · Ortho Diagnostics, Inc.

Substantially Equivalent

510(k) numberK790813

Submission

Device name
Multecon Blood Gas Control
Applicant
Ortho Diagnostics, Inc.
Mchenry, IL, US
Received
April 27, 1979
Decision date
June 28, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJS – Controls For Blood-Gases, (Assayed And Unassayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

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K033063Mission ControlsJJS · Traditional Diamond Diagnostics, Inc.12/12/2003SE
K022529Liquichek Blood Gas Plus Co-Oximeter Control (Il Synthesis Series) Levels 1,2, and 3…JJS · Traditional Bio-Rad08/15/2002SE
K022525Liquichek Blood Gas Plus Co-Oximeter Control (Radiometer 700 Series) Levels, 1,2 and 3…JJS · Traditional Bio-Rad08/15/2002SE
K003242Liquichek Blood Gas Plus Co-Oximeter Control (Il), Model 621,622,623JJS · Traditional Bio-Rad11/30/2000SE
K003239Liquichek Blood Gas Plus Co-Oximeter Control (800 Series), MODEL504,505,506JJS · Traditional Bio-Rad11/30/2000SE
K002866Liquichek Blood Gas Plus E Control Level 4, Model 574JJS · Traditional Bio-Rad09/25/2000SE

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Questions and answers

When was Multecon Blood Gas Control cleared by the FDA?

Multecon Blood Gas Control (K790813) received a 510(k) decision of Substantially Equivalent on June 28, 1979, 62 days after the submission was received.

What is the product code of K790813?

The FDA product code is JJS – Controls For Blood-Gases, (Assayed And Unassayed), a Class I (low risk) device regulated under 21 CFR 862.1660.