Medical Device Manufacturer · US , Ocala , FL

Zefon Intl. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Zefon Intl. Cardiovascular ✕

2 devices
1-2 of 2
Cleared Dec 19, 2008
VITALCHECK BLOOD PRESSURE CUFF, MODEL ZVC4000 SERIES
K082630 · DXQ
Cardiovascular · 100d
Cleared Jun 09, 2008
DURACHECK BLOOD PRESSURE CUFF, MODEL ZDC4000 SERIES
K080366 · DXQ
Cardiovascular · 118d
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