Bun-Reative

FDA 510(k) K760430 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK760430

Submission

Device name
Bun-Reative
Applicant
Boehringer Mannheim Corp.
Mchenry, IL, US
Received
August 13, 1976
Decision date
November 1, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CDS – Electrode, Ion Specific, Urea Nitrogen
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1770
Specialty
Clinical Chemistry

Other 510(k)s with product code CDS

510(k)DeviceApplicantDecision
K171247epoc Blood Urea Nitrogen Test, epoc Total Carbon Dioxide TestCDS · Traditional Epocal, Inc.01/17/2018SE
K040973Bun ReagentCDS · Traditional Genchem, Inc.12/27/2004SE
K033056Bun Reagent for Beckman Synchron CX & CX Delta ReagentCDS · Traditional Diamond Diagnostics, Inc.01/30/2004SE
K925550Hi Chem Bun Reagent Kit,Product Number 88806CDS · Traditional Hichem Diagnostics04/20/1993SE
K860543Blood Urea Nitrogen (Bun) TestcardCDS · Traditional Ilex Corp.04/21/1986SE
K855091Chem-Pro 1000 Clinical Chemistry-Analysis SysCDS · Traditional Sen Tech Medical Corp.03/14/1986SE
K812308Lancer Bun Rate Reagent KitCDS · Traditional Sherwood Medical Co.08/31/1981SE
K811193Bun Rate ReagentCDS · Traditional Chem-Elec, Inc.07/10/1981SE
K800616Bun Reagent Kit #88108CDS · Traditional Hi Chem, Inc.04/10/1980SE
K800590Bun KitCDS · Traditional Nobel Scientific Industries, Inc.04/04/1980SE

More from Nobel Scientific Industries, Inc.

510(k)DeviceDecision
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K983047Accu-Chek HQ SystemLFR · Traditional 02/05/1999SE
K984419Elecsys Ige CalcheckJJY · Traditional 02/02/1999SE
K984425Modification of Preciset Serum Proteins CalibratorJIX · Traditional 01/20/1999SE
K984372Elecsys Calcheck Troponin TJJY · Traditional 12/14/1998SE
K984105Elecsys Troponin T Stat TestMMI · Traditional 12/08/1998SE
K983503Roche Diagnostics, Boehringer Mannheim Corporation Inorganic Phosphorus Reagent Catalog…CEO · Traditional 12/01/1998SE
K983469Preciset Serum Proteins CalibratorJIX · Traditional 11/25/1998SE
K983185Boehringer Mannheim Tina-Quant Ige TestDGC · Traditional 11/12/1998SE
K983510Chemstrip 101 Urine AnalyzerKQO · Special 10/27/1998SE

Questions and answers

When was Bun-Reative cleared by the FDA?

Bun-Reative (K760430) received a 510(k) decision of Substantially Equivalent on November 1, 1976, 80 days after the submission was received.

What is the product code of K760430?

The FDA product code is CDS – Electrode, Ion Specific, Urea Nitrogen, a Class II (moderate risk) device regulated under 21 CFR 862.1770.