Medical Device Manufacturer · US , Sandy , UT

Becton Dickinson Vascular Access, Inc. - FDA 510(k) Cleared Devices

25 submissions · 22 cleared · Since 1992
25
Total
22
Cleared
0
Denied

Becton Dickinson Vascular Access, Inc. has 22 FDA 510(k) cleared general hospital devices. Based in Sandy, US.

Historical record: 22 cleared submissions from 1992 to 1997.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Becton Dickinson Vascular Access, Inc.

25 devices
1-12 of 25
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