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Guidewire 0.6 Single Use

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161940
510(k) Type
Special
Applicant
FIAGON GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/18/2016
Days to Decision
66 days
Submission Type
Summary

Guidewire 0.6 Single Use

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161940
510(k) Type
Special
Applicant
FIAGON GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/18/2016
Days to Decision
66 days
Submission Type
Summary