Ast (Got) Ifcc 2-VIAL Reagent W/Pyridoxyl Phosphat

FDA 510(k) K891468 · Trace Scientific , Ltd.

Substantially Equivalent

510(k) numberK891468

Submission

Device name
Ast (Got) Ifcc 2-VIAL Reagent W/Pyridoxyl Phosphat
Applicant
Trace Scientific , Ltd.
Clayton, Vic 3168, AU
Received
March 15, 1989
Decision date
May 22, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CIT – Nadh Oxidation/Nad Reduction, Ast/Sgot
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1100
Specialty
Clinical Chemistry

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K923322Trace Albumin-Mr ReagentCIX · Traditional 09/11/1992SE
K914731Trace Gamma Gt-Ss ReagentJQB · Traditional 11/19/1991SE
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Questions and answers

When was Ast (Got) Ifcc 2-VIAL Reagent W/Pyridoxyl Phosphat cleared by the FDA?

Ast (Got) Ifcc 2-VIAL Reagent W/Pyridoxyl Phosphat (K891468) received a 510(k) decision of Substantially Equivalent on May 22, 1989, 68 days after the submission was received.

What is the product code of K891468?

The FDA product code is CIT – Nadh Oxidation/Nad Reduction, Ast/Sgot, a Class II (moderate risk) device regulated under 21 CFR 862.1100.