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ARROW LARGE-BORE DUAL LUMEN HEMODIALYSIS KIT

Page Type
Cleared 510(K)
510(k) Number
K895417
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1990
Days to Decision
124 days

ARROW LARGE-BORE DUAL LUMEN HEMODIALYSIS KIT

Page Type
Cleared 510(K)
510(k) Number
K895417
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1990
Days to Decision
124 days