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CORDIS REUSABLE INFLATION DEVICE FOR ANGIOPLASTY

Page Type
Cleared 510(K)
510(k) Number
K863537
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/1986
Days to Decision
50 days

CORDIS REUSABLE INFLATION DEVICE FOR ANGIOPLASTY

Page Type
Cleared 510(K)
510(k) Number
K863537
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/1986
Days to Decision
50 days