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CATHETER,PERCUTANEOUS INTRODUC. & SHEATH

Page Type
Cleared 510(K)
510(k) Number
K770561
510(k) Type
Traditional
Applicant
USCI, DIV. C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1977
Days to Decision
34 days

CATHETER,PERCUTANEOUS INTRODUC. & SHEATH

Page Type
Cleared 510(K)
510(k) Number
K770561
510(k) Type
Traditional
Applicant
USCI, DIV. C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1977
Days to Decision
34 days