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ARROW KINK RESISTANT FLEXI-CATH INTRA-AORTIC BALLOON

Page Type
Cleared 510(K)
510(k) Number
K945230
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1995
Days to Decision
195 days
Submission Type
Statement

ARROW KINK RESISTANT FLEXI-CATH INTRA-AORTIC BALLOON

Page Type
Cleared 510(K)
510(k) Number
K945230
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1995
Days to Decision
195 days
Submission Type
Statement