Crospon, Ltd.

12 FDA 510(k) medical device clearances.

Top product codes for Crospon, Ltd.

FFX — Gastroenterology, Urology 7 devices
PIE — Gastroenterology, Urology 2 devices
FED — Gastroenterology, Urology 1 device
KNT — Gastroenterology, Urology 1 device
PID — Gastroenterology, Urology 1 device

Recent clearances by Crospon, Ltd.

K183072 — EndoFLIP System FFX · 2019-02-15
K172128 — EsoFLIP® ES-310 Balloon Catheter PIE · 2017-11-22
K170833 — EndoFLIP® System with FLIP Topography module FFX · 2017-04-17
K160725 — EndoFLIP FFX · 2016-05-01
K142000 — ESOFLIP ES PIE · 2014-09-25
K132337 — ESOFLIP BALLOON DILATION CATHETER PID · 2013-10-07
K130906 — ENDOFLIP CATHETER FFX · 2013-07-17
K120997 — BAROSTAT SOFTWARE OPTION FFX · 2012-08-27
K110531 — ENDOFLIP ECD FED · 2011-10-06
K110529 — ENDOFLIP GASTRIC TUBE KNT · 2011-07-22
K102214 — ENDO FLIP FFX · 2010-12-16
K092850 — ENDOFLIP FFX · 2009-12-15

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