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INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060302
510(k) Type
Traditional
Applicant
CORDIS EUROPA, N.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
4/11/2006
Days to Decision
64 days
Submission Type
Summary

INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060302
510(k) Type
Traditional
Applicant
CORDIS EUROPA, N.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
4/11/2006
Days to Decision
64 days
Submission Type
Summary