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BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843501
510(k) Type
Traditional
Applicant
ADVANCED CARDIOVASCULAR SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1984
Days to Decision
28 days

BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843501
510(k) Type
Traditional
Applicant
ADVANCED CARDIOVASCULAR SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1984
Days to Decision
28 days