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KISH URETHRAL ILLUMINATED CATHETER SET

Page Type
Cleared 510(K)
510(k) Number
K810367
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

KISH URETHRAL ILLUMINATED CATHETER SET

Page Type
Cleared 510(K)
510(k) Number
K810367
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