Spectrum Co-Oximeter Linearity Control

FDA 510(k) K945860 · Phoenix Diagnostics, Inc.

Substantially Equivalent

510(k) numberK945860

Submission

Device name
Spectrum Co-Oximeter Linearity Control
Applicant
Phoenix Diagnostics, Inc.
Natick, MA, US
Received
December 1, 1994
Decision date
January 17, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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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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
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K012509Phoenix Electrolyte Calibration Set for the Dade/Behring/Behring Dimension Chemistry…JIX · Traditional 10/09/2001SE
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K920285Blood Gas/Ise Linearity ControlJJS · Traditional 07/14/1992SE
K912718Enzyme Linearity ControlJJY · Traditional 09/06/1991SE

Questions and answers

When was Spectrum Co-Oximeter Linearity Control cleared by the FDA?

Spectrum Co-Oximeter Linearity Control (K945860) received a 510(k) decision of Substantially Equivalent on January 17, 1995, 47 days after the submission was received.

What is the product code of K945860?

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.