Bd

Bd — FDA 510(k) Submissions

Bd has submitted 15 FDA 510(k) premarket notifications since 2001, of which 15 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Devices Detecting Influenza A, B, And C Virus Antigens, Lavage, Jet, Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days, Allergen And Vaccine Delivery Needles, Needle, Hypodermic, Single Lumen . Use the specialty filter in the sidebar to narrow results.