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PERCUTANEOUS SURAPUBIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K780765
510(k) Type
Traditional
Applicant
VANCE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1978
Days to Decision
73 days

PERCUTANEOUS SURAPUBIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K780765
510(k) Type
Traditional
Applicant
VANCE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1978
Days to Decision
73 days