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RENAX A.V. FISTULA NEEDLE SETS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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