FDA 510(k) Applications for Medical Device Product Code "LZF"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K011238 | METRACOR TECHNOLOGIES, INC. | RODA (REAL TIME OXYGEN DYNAMICS ANALYSIS) MONITORING SYSTEM | 01/08/2002 |
K162042 | OPTISCAN BIOMEDICAL CORP. | OptiScanner 5000 Glucose Monitoring System | 10/16/2017 |
K192785 | Optiscan Biomedical Corporation | OptiScanner« 5000 Glucose Monitoring System | 02/05/2020 |
K951739 | VIA MEDICAL CORP. | PUMP/BLOOD CHEMISTRY MONITOR | 02/28/1996 |