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AV FISTULA NEEDLE SET

Page Type
Cleared 510(K)
510(k) Number
K771206
510(k) Type
Traditional
Applicant
TERUMO AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/1977
Days to Decision
10 days

AV FISTULA NEEDLE SET

Page Type
Cleared 510(K)
510(k) Number
K771206
510(k) Type
Traditional
Applicant
TERUMO AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/1977
Days to Decision
10 days