Schneider (Europe) GmbH

Schneider (Europe) GmbH holds 5 FDA 510(k) medical device clearances, first cleared 1995, most recent 1999.

Top product codes for Schneider (Europe) GmbH

DQX — Cardiovascular4 devices
ESW — General, Plastic Surgery1 device

Recent clearances by Schneider (Europe) GmbH

K984068 — FLAMINGO WALLSTENT ESOPHAGEAL ENDOPROSTHESISCode ESW·1999-01-07
K982592 — DOCKING-EXTENSION WIRECode DQX·1998-10-21
K970528 — CLYDE CORONARY GUIDEWIRECode DQX·1997-06-10
K970494 — HANNIBAL GUIDEWIRECode DQX·1997-05-09
K951109 — C-THRU CORONARY GUIDE WIRECode DQX·1995-06-08

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