Sooil Development Co., Ltd.

Sooil Development Co., Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 2000, most recent 2007.

Top product codes for Sooil Development Co., Ltd.

LZG — General Hospital3 devices
MRZ — General Hospital1 device

Recent clearances by Sooil Development Co., Ltd.

K071418 — DANA 3CC SYRINGE INSULIN RESERVOIRCode MRZ·2007-09-04
K063126 — DANA DIABECARE IISCode LZG·2007-02-02
K022317 — DANA DIABECARE II INSULIN PUMP & SUPERLINE-EASYRELEASE, SOFT-RELEASE-ST, & SOFT-RELEASE-R INFUSION SETSCode LZG·2002-08-02
K001604 — DANA DIABECARECode LZG·2000-08-14

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