Biotrol Total Protein H.P.

FDA 510(k) K882189 · Biotrol, USA, Inc.

Substantially Equivalent

510(k) numberK882189

Submission

Device name
Biotrol Total Protein H.P.
Applicant
Biotrol, USA, Inc.
Malvern, PA, US
Received
May 24, 1988
Decision date
July 1, 1988
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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K971524Total Protein or TPCEK · Traditional Carolina Liquid Chemistries Corp.05/16/1997SE
K961864Csf/Urine Total ProteinCEK · Traditional Teco Diagnostics10/24/1996SE
K955905STC Diagnostics Auto-Lyte Urinary Protein AssayCEK · Traditional Solarcare Technologies Corp,Inc.05/30/1996SE
K955936Total Protein ReagentCEK · Traditional Derma Media Lab., Inc.03/12/1996SE
K950920Dupont Dimension Total Protein MethodCEK · Traditional Dupont Medical Products08/11/1995SE
K950234Total Protein Test (Tpro) Item Number: XXXXX/R1. R2CEK · Traditional Emd Chemicals, Inc.06/14/1995SE
K950128Total Protein Test (Tpro) Item XXXXX/R1. R2CEK · Traditional Emd Chemicals, Inc.05/15/1995SE

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Questions and answers

When was Biotrol Total Protein H.P. cleared by the FDA?

Biotrol Total Protein H.P. (K882189) received a 510(k) decision of Substantially Equivalent on July 1, 1988, 38 days after the submission was received.

What is the product code of K882189?

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