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UNITIP HIGH RESOLUTION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062222
510(k) Type
Traditional
Applicant
UNISENSOR AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2007
Days to Decision
225 days
Submission Type
Summary

UNITIP HIGH RESOLUTION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062222
510(k) Type
Traditional
Applicant
UNISENSOR AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2007
Days to Decision
225 days
Submission Type
Summary