Neoseed Technology,Llc

Neoseed Technology,Llc holds 1 FDA 510(k) medical device clearance, cleared in 2002.

Top product codes for Neoseed Technology,Llc

FGI — Gastroenterology, Urology1 device

Recent clearances by Neoseed Technology,Llc

K013360 — DFINER UROLOGICAL CATHETERCode FGI·2002-02-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.