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Radifocus Glidewire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152740
510(k) Type
Traditional
Applicant
ASHITAKA FACTORY OF TERUMO CORP.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
11/16/2015
Days to Decision
54 days
Submission Type
Summary

Radifocus Glidewire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152740
510(k) Type
Traditional
Applicant
ASHITAKA FACTORY OF TERUMO CORP.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
11/16/2015
Days to Decision
54 days
Submission Type
Summary