Angiologica B. M. Srl

Angiologica B. M. Srl holds 2 FDA 510(k) medical device clearances, first cleared 2005, most recent 2009.

Top product codes for Angiologica B. M. Srl

FER — Gastroenterology, Urology1 device
FTL — General, Plastic Surgery1 device

Recent clearances by Angiologica B. M. Srl

K090432 — HEMORPEX SYSTEMCode FER·2009-05-29
K043191 — REPOL ANGIMESH, ANGIMESH PRE, FOLDED MESH, REPOL PLUG BASIC, REPOL PLUG CAP, REPOL PLUG FLOWER AND WINGS MESHCode FTL·2005-05-16

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