Single Vial Lipase Test Kit
FDA 510(k) K802842 · Biodynamics Corp.
510(k) numberK802842
Submission
- Device name
- Single Vial Lipase Test Kit
- Applicant
- Biodynamics Corp.
Mchenry, IL, US - Received
- November 12, 1980
- Decision date
- December 18, 1980
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- CHI – Lipase-Esterase, Enzymatic, Photometric, Lipase
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.1465
- Specialty
- Clinical Chemistry
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|---|---|---|---|
| K970905 | Synchron CX Systems Lipase (Lipa) ReagentCHI · Traditional | Beckman Instruments, Inc. | 06/04/1997SE |
| K961179 | Sentinel Lipase Liquid Model 17.401BCHI · Traditional | Equal Diagnostics, Inc. | 07/19/1996SE |
| K952180 | CX Lipase Reagent & Calibrator for Synchron CX SystemsCHI · Traditional | Beckman Instruments, Inc. | 08/17/1995SE |
| K952816 | Lipase Flex Reagent CartridgeCHI · Traditional | Dupont Medical Products | 07/20/1995SE |
| K952647 | Il Test LipaseCHI · Traditional | Instrumentation Laboratory CO | 07/20/1995SE |
| K941085 | Lipase-Ps Assay Procedure No. 805CHI · Traditional | Sigma Diagnostics, Inc. | 05/17/1994SE |
| K923917 | Elipase Human Pancreatic Lipase EnzymeimmunoassayCHI · Traditional | Nuclear Diagnostics, Inc. | 02/25/1994SE |
| K921249 | Wako Autokit Lipase-ColorCHI · Traditional | Wako Chemicals USA, Inc. | 07/21/1992SE |
| K920337 | Miles Lipase Sera-Pak MethodCHI · Traditional | Heraeus Kulzer, Inc. | 03/11/1992SE |
| K900827 | Colorimetric Chloride Product #4314125CHI · Traditional | American Research Products Co. | 05/02/1990SE |
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| K874034 | ADR-22 Automatic Dialyzer ReprocessorLIF · Traditional | 10/23/1987SE |
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| K822716 | Universal CentrifugeJPI · Traditional | 09/30/1982SE |
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Questions and answers
When was Single Vial Lipase Test Kit cleared by the FDA?
Single Vial Lipase Test Kit (K802842) received a 510(k) decision of Substantially Equivalent on December 18, 1980, 36 days after the submission was received.
What is the product code of K802842?
The FDA product code is CHI – Lipase-Esterase, Enzymatic, Photometric, Lipase, a Class I (low risk) device regulated under 21 CFR 862.1465.