Ventlab Corp. - FDA 510(k) Cleared Devices
Recent clearances: VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER, CUFF SENTRY, VENTLAB 6000 SERIES HUMIDIFIER
22
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ventlab Corp. General & Plastic Surgery ✕
1 devices