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AV FISTULA NEEDLE SET

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