Calcium (Az III) Reagent

FDA 510(k) K922835 · King Diagnostics, Inc.

Substantially Equivalent

510(k) numberK922835

Submission

Device name
Calcium (Az III) Reagent
Applicant
King Diagnostics, Inc.
Indianapolis, IN, US
Received
June 12, 1992
Decision date
August 4, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CJY – Azo Dye, Calcium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1145
Specialty
Clinical Chemistry

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More from Ortho-Clinical Diagnostics, Inc.

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K931773HDL Precipitating Reagent (Dextran Sulfate)LBR · Traditional 08/16/1993SE
K931326King Diagnostics CK ReagentCGS · Traditional 06/15/1993SE
K923129King Diagnostics Glucose (HK) ReagentCFR · Traditional 11/02/1992SE
K922969King Diagnostics Urea Nitrogen ReagentCDN · Traditional 10/13/1992SE
K922921King Diagnostics Chloride ReagentCHJ · Traditional 10/05/1992SE
K923927King Diagnostics Magnesium ReagentJGJ · Traditional 09/30/1992SE
K923128King Diagnostics Cholesterol ReagentCHH · Traditional 09/09/1992SE
K923091King Diagnostics Gamma GT ReagentJPZ · Traditional 09/09/1992SE

Questions and answers

When was Calcium (Az III) Reagent cleared by the FDA?

Calcium (Az III) Reagent (K922835) received a 510(k) decision of Substantially Equivalent on August 4, 1992, 53 days after the submission was received.

What is the product code of K922835?

The FDA product code is CJY – Azo Dye, Calcium, a Class II (moderate risk) device regulated under 21 CFR 862.1145.