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NOVOSTE VESSEL DILATER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912050
510(k) Type
Traditional
Applicant
NOVASTE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/1991
Days to Decision
153 days
Submission Type
Statement

NOVOSTE VESSEL DILATER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912050
510(k) Type
Traditional
Applicant
NOVASTE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/1991
Days to Decision
153 days
Submission Type
Statement