Synchron CX Systems Glucose Reagent (Glu)

FDA 510(k) K971467 · Carolina Liquid Chemistries Corp.

Substantially Equivalent

510(k) numberK971467

Submission

Device name
Synchron CX Systems Glucose Reagent (Glu)
Applicant
Carolina Liquid Chemistries Corp.
Brea, CA, US
Received
April 22, 1997
Decision date
June 16, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CFR – Hexokinase, Glucose
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1345
Specialty
Clinical Chemistry

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Questions and answers

When was Synchron CX Systems Glucose Reagent (Glu) cleared by the FDA?

Synchron CX Systems Glucose Reagent (Glu) (K971467) received a 510(k) decision of Substantially Equivalent on June 16, 1997, 55 days after the submission was received.

What is the product code of K971467?

The FDA product code is CFR – Hexokinase, Glucose, a Class II (moderate risk) device regulated under 21 CFR 862.1345.