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VEIN GRAFT CANNULA

Page Type
Cleared 510(K)
510(k) Number
K791832
510(k) Type
Traditional
Applicant
D/P, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1979
Days to Decision
16 days

VEIN GRAFT CANNULA

Page Type
Cleared 510(K)
510(k) Number
K791832
510(k) Type
Traditional
Applicant
D/P, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1979
Days to Decision
16 days