QUALICHECK5+ Models S7730, S7740, S7750, S7760

FDA 510(k) K980135 · Radiometer America, Inc.

Substantially Equivalent

510(k) numberK980135

Submission

Device name
QUALICHECK5+ Models S7730, S7740, S7750, S7760
Applicant
Radiometer America, Inc.
Westlake, OH, US
Received
January 15, 1998
Decision date
January 28, 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
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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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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Questions and answers

When was QUALICHECK5+ Models S7730, S7740, S7750, S7760 cleared by the FDA?

QUALICHECK5+ Models S7730, S7740, S7750, S7760 (K980135) received a 510(k) decision of Substantially Equivalent on January 28, 1998, 13 days after the submission was received.

What is the product code of K980135?

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.