In-Vitro Test Determination of Sgot (Ast)
FDA 510(k) K854187 · Clinical Data, Inc.
510(k) numberK854187
Submission
- Device name
- In-Vitro Test Determination of Sgot (Ast)
- Applicant
- Clinical Data, Inc.
Boston, MA, US - Received
- October 15, 1985
- Decision date
- November 25, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- CIS – Hydrazone Colorimetry, Ast/Sgot
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1100
- Specialty
- Clinical Chemistry
Other 510(k)s with product code CIS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K032027 | Cholestech LDX Aspartate Aminotransferase (Ast)CIS · Traditional | Cholestech Corp. | 09/05/2003SE |
| K896238 | Cobas Ready Ast ReagentCIS · Traditional | Roche Diagnostic Systems, Inc. | 02/16/1990SE |
| K812872 | Optional Total Ca-Module for Il 504/508CIS · Traditional | Instrumentation Laboratory CO | 10/26/1981SE |
| K792410 | Elvi Sgot & SGPT TransaminaseCIS · Traditional | Volu Sol Medical Industries | 12/06/1979SE |
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Questions and answers
When was In-Vitro Test Determination of Sgot (Ast) cleared by the FDA?
In-Vitro Test Determination of Sgot (Ast) (K854187) received a 510(k) decision of Substantially Equivalent on November 25, 1985, 41 days after the submission was received.
What is the product code of K854187?
The FDA product code is CIS – Hydrazone Colorimetry, Ast/Sgot, a Class II (moderate risk) device regulated under 21 CFR 862.1100.