Ventrex Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SPECIFIC IGE EIA-TURBO ASSAY, VENTREX ALLERGEN DISC, VENTREX COATED TUBE INTACT PTH
82
Total
82
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ventrex Laboratories, Inc. Hematology ✕
2 devices