Determination of Quinidine
FDA 510(k) K860049 · Clinical Data, Inc.
510(k) numberK860049
Submission
- Device name
- Determination of Quinidine
- Applicant
- Clinical Data, Inc.
Boston, MA, US - Received
- January 6, 1986
- Decision date
- January 22, 1986
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- LBZ – Enzyme Immunoassay, Quinidine
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3320
- Specialty
- Clinical Toxicology
Other 510(k)s with product code LBZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K052826 | QMS Quinidine. QMS Quinidine CalibratorsLBZ · Traditional | Seradyn, Inc. | 12/23/2005SE |
| K032332 | Roche Online TDM QuinidineLBZ · Traditional | Roche Diagnostics Corp. | 01/12/2004SE |
| K011605 | Emit 2000 Quinidine Assay, Model OSR4Q229LBZ · Special | Syva Co., Dade Behring, Inc. | 06/12/2001SE |
| K964116 | Quinidine Assay for the Technicon Immuno 1 System (in Vitro Diagnostic System)LBZ · Traditional | Bayer Corp. | 12/24/1996SE |
| K964212 | Quinidine Enzyme ImmunoassayLBZ · Traditional | Diagnostic Reagents, Inc. | 12/18/1996SE |
| K955568 | Innofluor Quinidine Assay SystemLBZ · Traditional | Oxis Intl., Inc. | 04/04/1996SE |
| K941440 | Cobas-Fp Quinidine Reagents and CalibratorsLBZ · Traditional | Roche Diagnostic Systems, Inc. | 07/06/1994SE |
| K922913 | Emit 2000 Quindine Assay Quididine CalibratorsLBZ · Traditional | Syva Co. | 08/24/1992SE |
| K904990 | Emit Convenience Pack, Quinidine Assay/CalibratorsLBZ · Traditional | Syva Co. | 02/04/1991SE |
| K900705 | Modified Accufluor Quinidine Reagent & CalibratorLBZ · Traditional | Innotron of Oregon, Inc. | 04/12/1990SE |
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| K033983 | Vitalab Iron ReagentJIY · Traditional | 05/21/2004SE |
| K040631 | Vitalab Direct Bilirubin ReagentCIG · Traditional | 03/18/2004SE |
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| K034000 | Vitalab Triglycerides Reagent and Vitalab CalibratorCDT · Traditional | 03/10/2004SE |
| K040508 | Vitalab Magnesium ReagentJGJ · Traditional | 03/08/2004SE |
| K040467 | Vitalab Uric Acid ReagentKNK · Traditional | 03/08/2004SE |
| K031042 | Atac Hemoglobin A1C Reagent KitLCP · Traditional | 11/03/2003SE |
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Questions and answers
When was Determination of Quinidine cleared by the FDA?
Determination of Quinidine (K860049) received a 510(k) decision of Substantially Equivalent on January 22, 1986, 16 days after the submission was received.
What is the product code of K860049?
The FDA product code is LBZ – Enzyme Immunoassay, Quinidine, a Class II (moderate risk) device regulated under 21 CFR 862.3320.