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HANCOCK AORTIC PUNCH

Page Type
Cleared 510(K)
510(k) Number
K800122
510(k) Type
Traditional
Applicant
HANCOCK LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/1980
Days to Decision
14 days

HANCOCK AORTIC PUNCH

Page Type
Cleared 510(K)
510(k) Number
K800122
510(k) Type
Traditional
Applicant
HANCOCK LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/1980
Days to Decision
14 days