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A.V. FISTULA NEEDLE SET

Page Type
Cleared 510(K)
510(k) Number
K782021
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1979
Days to Decision
106 days

A.V. FISTULA NEEDLE SET

Page Type
Cleared 510(K)
510(k) Number
K782021
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1979
Days to Decision
106 days