Crospon, Ltd.

Crospon, Ltd. holds 12 FDA 510(k) medical device clearances, first cleared 2009, most recent 2019.

Top product codes for Crospon, Ltd.

FFX — Gastroenterology, Urology7 devices
PIE — Gastroenterology, Urology2 devices
FED — Gastroenterology, Urology1 device
KNT — Gastroenterology, Urology1 device
PID — Gastroenterology, Urology1 device

Recent clearances by Crospon, Ltd.

K183072 — EndoFLIP SystemCode FFX·2019-02-15
K172128 — EsoFLIP® ES-310 Balloon CatheterCode PIE·2017-11-22
K170833 — EndoFLIP® System with FLIP Topography moduleCode FFX·2017-04-17
K160725 — EndoFLIPCode FFX·2016-05-01
K142000 — ESOFLIP ESCode PIE·2014-09-25
K132337 — ESOFLIP BALLOON DILATION CATHETERCode PID·2013-10-07
K130906 — ENDOFLIP CATHETERCode FFX·2013-07-17
K120997 — BAROSTAT SOFTWARE OPTIONCode FFX·2012-08-27
K110531 — ENDOFLIP ECDCode FED·2011-10-06
K110529 — ENDOFLIP GASTRIC TUBECode KNT·2011-07-22
K102214 — ENDO FLIPCode FFX·2010-12-16
K092850 — ENDOFLIPCode FFX·2009-12-15

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