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VANCE URETHAL DILATOR SET

Page Type
Cleared 510(K)
510(k) Number
K810371
510(k) Type
Traditional
Applicant
VANCE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1981
Days to Decision
36 days

VANCE URETHAL DILATOR SET

Page Type
Cleared 510(K)
510(k) Number
K810371
510(k) Type
Traditional
Applicant
VANCE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1981
Days to Decision
36 days