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PERCUTANEOUS SHEATH INTRODUCER KIT

Page Type
Cleared 510(K)
510(k) Number
K780532
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1978
Days to Decision
17 days

PERCUTANEOUS SHEATH INTRODUCER KIT

Page Type
Cleared 510(K)
510(k) Number
K780532
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1978
Days to Decision
17 days