Zefon Intl. - FDA 510(k) Cleared Devices
Recent clearances: VITALCHECK BLOOD PRESSURE CUFF, MODEL ZVC4000 SERIES, DURACHECK BLOOD PRESSURE CUFF, MODEL ZDC4000 SERIES
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Zefon Intl. Cardiovascular ✕
2 devices