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MODIFIED ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K896690
510(k) Type
Traditional
Applicant
NOVOSTE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1990
Days to Decision
57 days

MODIFIED ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K896690
510(k) Type
Traditional
Applicant
NOVOSTE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1990
Days to Decision
57 days