Diazyme Ldl-Cholesterol Reagent, Calibrator and Controls
FDA 510(k) K072523 · General Atomics
510(k) numberK072523
Submission
- Device name
- Diazyme Ldl-Cholesterol Reagent, Calibrator and Controls
- Applicant
- General Atomics
Poway, CA, US - Received
- September 7, 2007
- Decision date
- January 22, 2008
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LBR – Ldl & Vldl Precipitation, Hdl
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.1475
- Specialty
- Clinical Chemistry
Other 510(k)s with product code LBR
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K143691 | LDLC3 LDL-Cholesterol Gen.3LBR · Traditional | Roche Diagnostics Operations (Rdo) | 01/28/2015SE |
| K050823 | Direct HDL Cholesterol and Direct Hdl/Ldl CalibratorLBR · Traditional | Teco Diagnostics | 07/26/2005SE |
| K023784 | Raichem HDL Cholesterol Using Cantrol HDL Precipitating Tubes on the Cobas Mira AnaylzerLBR · Special | Hemagen Diagnostics, Inc. | 12/24/2002SE |
| K012593 | Vitros Chemistry Products Magnetic Hdl-Cholesterol Reagent, Vitros Chemistry Products…LBR · Special | Ortho-Clinical Diagnostics, Inc. | 08/30/2001SE |
| K992029 | Atac Direct HDL Cholesterol Reagent and Atac Hdl-C Calibrator KitsLBR · Traditional | Elan Diagnostics | 08/12/1999SE |
| K992002 | Autohdl Cholesterol Reagent SetLBR · Traditional | Pointe Scientific, Inc., | 08/05/1999SE |
| K991789 | Atac-Pak Direct HDL Cholesterol Reagent and Atac Hdl-C Calibrator KitsLBR · Traditional | Elan Holdings, Inc. | 07/09/1999SE |
| K990247 | MTM Bioscanner HDL, Model # BSA450, BSA460, BSA470LBR · Traditional | Polymer Technology Systems, Inc. | 05/28/1999SE |
| K984303 | Vitros Chemistry Products Magnetic Hdl-Cholesterol ReagentLBR · Traditional | Ortho-Clinical Diagnostics, Inc. | 01/28/1999SE |
| K980772 | Hdl-Cholesterol Precipitating Reagent, Catalogue Number 205-51LBR · Traditional | Diagnostic Chemicals , Ltd. | 04/27/1998SE |
More from Diagnostic Chemicals , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K082488 | Diazyme Lp(A) AssayDFC · Traditional | 01/13/2009SE |
| K072977 | Diazyme Apolipoprotein A-1 AssayMSJ · Traditional | 07/16/2008SE |
| K050178 | HBA1C Enzymatic AssayLCP · Traditional | 06/28/2005SE |
| K042448 | Diazyme Homocysteine Enzymatic Assay KitJJX · Traditional | 10/29/2004SE |
| K033360 | Diazyme Lithium Enzymatic Assay KitJII · Traditional | 12/23/2003SE |
Questions and answers
When was Diazyme Ldl-Cholesterol Reagent, Calibrator and Controls cleared by the FDA?
Diazyme Ldl-Cholesterol Reagent, Calibrator and Controls (K072523) received a 510(k) decision of Substantially Equivalent on January 22, 2008, 137 days after the submission was received.
What is the product code of K072523?
The FDA product code is LBR – Ldl & Vldl Precipitation, Hdl, a Class I (low risk) device regulated under 21 CFR 862.1475.