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ARROW SHEATHLESS INTRA-AORTIC BALLOON CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961358
510(k) Type
Traditional
Applicant
Arrow Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/1996
Days to Decision
85 days
Submission Type
Statement

ARROW SHEATHLESS INTRA-AORTIC BALLOON CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961358
510(k) Type
Traditional
Applicant
Arrow Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/1996
Days to Decision
85 days
Submission Type
Statement