Denka Seiken Co., Ltd.

Denka Seiken Co., Ltd. holds 6 FDA 510(k) medical device clearances, first cleared 2003, most recent 2017.

Top product codes for Denka Seiken Co., Ltd.

Recent clearances by Denka Seiken Co., Ltd.

K161679 — s LDL-EX SEIKENCode PYP·2017-08-18
K060359 — ARCHIECT INSULIN AND CONTROLS, MODEL 8K41-01, 8K41-10Code JIT·2006-04-14
K043264 — LDL-EX SEIKEN ASSAY KITCode MRR·2005-01-26
K041090 — HDL-EX SEIKEN ASSAY KITCode LBS·2004-10-29
K030545 — CRP-LATEX (II)X2 SEIKEN ASSAY KITCode DCK·2003-06-02
K030546 — CRP (II) CALIBRATORSCode JIS·2003-06-02

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