Spectrum Vascular

Spectrum Vascular — FDA 510(k) Submissions

Spectrum Vascular has submitted 3 FDA 510(k) premarket notifications since 2024, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days, Needle, Hypodermic, Single Lumen, Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days . Use the specialty filter in the sidebar to narrow results.