Sunder Biomedical Tech. Co., Ltd.

Sunder Biomedical Tech. Co., Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 2001, most recent 2003.

Top product codes for Sunder Biomedical Tech. Co., Ltd.

Recent clearances by Sunder Biomedical Tech. Co., Ltd.

K024007 — SUNDER CENTRAL VENOUS CATHETER KIT, MODELS SD-3L55F30J AND SD-3L70F30JCode FOZ·2003-07-14
K014140 — RENAX HEMODIALYSIS BLOOD TUBING SET; SUNDER HEMODIALYSIS BLOOD TUBING SETCode FJK·2002-11-18
K003123 — RENAX A.V. FISTULA NEEDLE SETSCode FIE·2001-05-04

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