FDA 510(k) Applications Submitted by SUNDER BIOMEDICAL TECH. CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K003123 10/05/2000 RENAX A.V. FISTULA NEEDLE SETS SUNDER BIOMEDICAL TECH. CO., LTD.
K024007 12/04/2002 SUNDER CENTRAL VENOUS CATHETER KIT, MODELS SD-3L55F30J AND SD-3L70F30J SUNDER BIOMEDICAL TECH. CO., LTD.
K014140 12/17/2001 RENAX HEMODIALYSIS BLOOD TUBING SET; SUNDER HEMODIALYSIS BLOOD TUBING SET SUNDER BIOMEDICAL TECH. CO., LTD.


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