RA-1000 System Add'L Analytes Phase III

FDA 510(k) K820913 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK820913

Submission

Device name
RA-1000 System Add'L Analytes Phase III
Applicant
Technicon Instruments Corp.
Mchenry, IL, US
Received
April 1, 1982
Decision date
May 3, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CEK – Biuret (Colorimetric), Total Protein
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1635
Specialty
Clinical Chemistry

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K950128Total Protein Test (Tpro) Item XXXXX/R1. R2CEK · Traditional Emd Chemicals, Inc.05/15/1995SE

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Questions and answers

When was RA-1000 System Add'L Analytes Phase III cleared by the FDA?

RA-1000 System Add'L Analytes Phase III (K820913) received a 510(k) decision of Substantially Equivalent on May 3, 1982, 32 days after the submission was received.

What is the product code of K820913?

The FDA product code is CEK – Biuret (Colorimetric), Total Protein, a Class II (moderate risk) device regulated under 21 CFR 862.1635.