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INSCOPE 3-STAGE BALLOON DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043605
510(k) Type
Traditional
Applicant
CORDIS EUROPA, N.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
2/4/2005
Days to Decision
36 days
Submission Type
Summary

INSCOPE 3-STAGE BALLOON DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043605
510(k) Type
Traditional
Applicant
CORDIS EUROPA, N.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
2/4/2005
Days to Decision
36 days
Submission Type
Summary