Flexicath , Ltd.

Flexicath , Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 2007, most recent 2012.

Top product codes for Flexicath , Ltd.

FOZ — General Hospital3 devices
LJS — General Hospital1 device

Recent clearances by Flexicath , Ltd.

K111939 — M/29TM - PRESSURE INJECTABLECode FOZ·2012-07-11
K092629 — SNM FIRMGRIPCode FOZ·2009-09-25
K080793 — FIRMGRIPCode FOZ·2008-10-16
K063363 — FIRMGRIP PERIPHERALLY INSERTED CATHETER DEVICECode LJS·2007-05-07

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