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RENAX A.V. FISTULA NEEDLE SETS

Page Type
Cleared 510(K)
510(k) Number
K003123
510(k) Type
Traditional
Applicant
SUNDER BIOMEDICAL TECH. CO., LTD.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
5/4/2001
Days to Decision
211 days
Submission Type
Summary

RENAX A.V. FISTULA NEEDLE SETS

Page Type
Cleared 510(K)
510(k) Number
K003123
510(k) Type
Traditional
Applicant
SUNDER BIOMEDICAL TECH. CO., LTD.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
5/4/2001
Days to Decision
211 days
Submission Type
Summary