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MODIFIED CATHETER PACKAGE

Page Type
Cleared 510(K)
510(k) Number
K800703
510(k) Type
Traditional
Applicant
HANCOCK LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/1980
Days to Decision
12 days

MODIFIED CATHETER PACKAGE

Page Type
Cleared 510(K)
510(k) Number
K800703
510(k) Type
Traditional
Applicant
HANCOCK LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/1980
Days to Decision
12 days