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VANCE KIDNEY BIOPSY BRUSHES

Page Type
Cleared 510(K)
510(k) Number
K792220
510(k) Type
Traditional
Applicant
VANCE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/1979
Days to Decision
31 days

VANCE KIDNEY BIOPSY BRUSHES

Page Type
Cleared 510(K)
510(k) Number
K792220
510(k) Type
Traditional
Applicant
VANCE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/1979
Days to Decision
31 days