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SCANLAN SINGLE-USE AORTA PUNCH

Page Type
Cleared 510(K)
510(k) Number
K823764
510(k) Type
Traditional
Applicant
SCANLAN INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1983
Days to Decision
100 days

SCANLAN SINGLE-USE AORTA PUNCH

Page Type
Cleared 510(K)
510(k) Number
K823764
510(k) Type
Traditional
Applicant
SCANLAN INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1983
Days to Decision
100 days