Bio-Rad Serum Proteins by Capillary Electrophoresis

FDA 510(k) K963018 · Bio-Rad

Substantially Equivalent

510(k) numberK963018

Submission

Device name
Bio-Rad Serum Proteins by Capillary Electrophoresis
Applicant
Bio-Rad
Hercules, CA, US
Received
August 2, 1996
Decision date
June 4, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CEF – Electrophoretic, Protein Fractionation
Device class
Class I (low risk)
Regulation
21 CFR 862.1630
Specialty
Clinical Chemistry

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Questions and answers

When was Bio-Rad Serum Proteins by Capillary Electrophoresis cleared by the FDA?

Bio-Rad Serum Proteins by Capillary Electrophoresis (K963018) received a 510(k) decision of Substantially Equivalent on June 4, 1997, 306 days after the submission was received.

What is the product code of K963018?

The FDA product code is CEF – Electrophoretic, Protein Fractionation, a Class I (low risk) device regulated under 21 CFR 862.1630.