INNOFLUOR QUINIDINE ASSAY SYSTEM
Device Facts
| Record ID | K955568 |
|---|---|
| Device Name | INNOFLUOR QUINIDINE ASSAY SYSTEM |
| Applicant | Oxis Intl., Inc. |
| Product Code | LBZ · Clinical Toxicology |
| Decision Date | Apr 4, 1996 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 862.3320 |
| Device Class | Class 2 |
Intended Use
The INNOFLUOR™ Quinidine Assay System (Modified) is intended for the quantitative measurement of quinidine in human serum.
Device Story
In vitro diagnostic assay; measures quinidine concentrations in human serum; performed on Abbott TDx® analyzer; used by laboratory personnel for therapeutic drug monitoring; results used by clinicians to assess patient quinidine levels; aids in optimizing dosage and managing toxicity.
Clinical Evidence
Bench testing only. Comparison of 49 serum patient samples between INNOFLUOR™ and Abbott Quinidine Assay. Linear regression: y = 0.958x - 0.077; correlation coefficient r = 0.986.
Technological Characteristics
In vitro diagnostic reagent system; quantitative assay; designed for use on Abbott TDx® analyzer; utilizes established immunoassay principles for quinidine detection.
Indications for Use
Indicated for quantitative measurement of quinidine in human serum for therapeutic drug monitoring.
Regulatory Classification
Identification
A digoxin test system is a device intended to measure digoxin, a cardiovascular drug, in serum and plasma. Measurements obtained by this device are used in the diagnosis and treatment of digoxin overdose and in monitoring levels of digoxin to ensure appropriate therapy.
Predicate Devices
- INNOFLUOR™ Quinidine Reagent Set (Existing)
- Abbott Quinidine Assay
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