Last synced on 18 July 2025 at 11:06 pm

HANCOCK AORTIC PUNCH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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