Schneider U.S. Stent Div.

Schneider U.S. Stent Div. holds 3 FDA 510(k) medical device clearances, first cleared 1991, most recent 1994.

Top product codes for Schneider U.S. Stent Div.

FGE — Gastroenterology, Urology2 devices
ESW — General, Plastic Surgery1 device

Recent clearances by Schneider U.S. Stent Div.

K923993 — WALLSTENT BILIARY ENDOPROTHESESCode FGE·1994-09-30
K923119 — WALLSTENT ESOPHAGEAL PROTHESISCode ESW·1992-09-01
K914277 — WALLSTENT(R) TRANS BILIARY ENDO W/UNISTEP DELIV SYCode FGE·1991-11-29

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