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PERCUTANEOUS TRANSLUMINAL BLOOD DILATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K851848
510(k) Type
Traditional
Applicant
MANSFIELD SCIENTIFIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/1985
Days to Decision
84 days

PERCUTANEOUS TRANSLUMINAL BLOOD DILATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K851848
510(k) Type
Traditional
Applicant
MANSFIELD SCIENTIFIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/1985
Days to Decision
84 days