Blood Urea Nitrogen Reagent Sys

FDA 510(k) K840213 · Sclavo, Inc.

Substantially Equivalent

510(k) numberK840213

Submission

Device name
Blood Urea Nitrogen Reagent Sys
Applicant
Sclavo, Inc.
Mchenry, IL, US
Received
January 19, 1984
Decision date
March 19, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JGZ – O-Phthalaldehyde, Urea Nitrogen
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1770
Specialty
Clinical Chemistry

Other 510(k)s with product code JGZ

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K883327Clinistat Bun (Blood Urea Nitrogen) Reagent TestJGZ · Traditional Heraeus Kulzer, Inc.01/23/1989SE
K863901Iq Urea NitrogenJGZ · Traditional Bd Becton Dickinson Vacutainer Systems Preanalytic11/24/1986SE
K842772Pharmacia B2-MICRO RiaJGZ · Traditional Pharmacia, Inc.11/01/1984SE
K820418K.D. Colorimetric Blood Urea N2 TestJGZ · Traditional King Diagnostics, Inc.03/11/1982SE
K810087Urea Nitrogen, KineticJGZ · Traditional Bio-Analytics Laboratories, Inc.02/26/1981SE
K801269Seralyzer Blood Urea Nitrogen(Bun)JGZ · Traditional Miles Laboratories, Inc.07/08/1980SE
K792362Blood Urea Nitrogen ReagentJGZ · Traditional Connecticut Diagnostics, Ltd.12/06/1979SE
K770504Reagent SystemJGZ · Traditional American Monitor Corp.06/27/1977SE

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Questions and answers

When was Blood Urea Nitrogen Reagent Sys cleared by the FDA?

Blood Urea Nitrogen Reagent Sys (K840213) received a 510(k) decision of Substantially Equivalent on March 19, 1984, 60 days after the submission was received.

What is the product code of K840213?

The FDA product code is JGZ – O-Phthalaldehyde, Urea Nitrogen, a Class II (moderate risk) device regulated under 21 CFR 862.1770.