Medical Device Manufacturer · US , Franklin Lakes , NJ

Bd/Preefil - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000

Total

Cleared

Denied

Bd/Preefil has 1 FDA 510(k) cleared medical devices. Based in Franklin Lakes, US.

Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Bd/Preefil Filter by specialty or product code using the sidebar.

Bd/Preefil is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Bd/Preefil

1 devices

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