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ARROW M.I.S. MULTI-LUMEN CATHETERIZA

Page Type
Cleared 510(K)
510(k) Number
K820648
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1982
Days to Decision
36 days

ARROW M.I.S. MULTI-LUMEN CATHETERIZA

Page Type
Cleared 510(K)
510(k) Number
K820648
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1982
Days to Decision
36 days