Sigma Diagnostics CX -3 Calibration Standard, Level 2

FDA 510(k) K963543 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK963543

Submission

Device name
Sigma Diagnostics CX -3 Calibration Standard, Level 2
Applicant
Sigma Diagnostics, Inc.
St. Louis, MO, US
Received
September 4, 1996
Decision date
October 30, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JIX – Calibrator, Multi-Analyte Mixture
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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Questions and answers

When was Sigma Diagnostics CX -3 Calibration Standard, Level 2 cleared by the FDA?

Sigma Diagnostics CX -3 Calibration Standard, Level 2 (K963543) received a 510(k) decision of Substantially Equivalent on October 30, 1996, 56 days after the submission was received.

What is the product code of K963543?

The FDA product code is JIX – Calibrator, Multi-Analyte Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.1150.