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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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