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THEROX INFUSION GUIDEWIRES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971719
510(k) Type
Traditional
Applicant
Therox, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1997
Days to Decision
178 days
Submission Type
Summary

THEROX INFUSION GUIDEWIRES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971719
510(k) Type
Traditional
Applicant
Therox, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1997
Days to Decision
178 days
Submission Type
Summary