Medical Device Manufacturer · US , Rockville , MD

Dyn-Bioshaf (2006) , Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2007

Total

Cleared

Denied

Dyn-Bioshaf (2006) , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Rockville, US.

Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Dyn-Bioshaf (2006) , Ltd. Filter by specialty or product code using the sidebar.

Dyn-Bioshaf (2006) , Ltd. 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 - Dyn-Bioshaf (2006) , Ltd.

1 devices

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