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REFORM PERIPHERAL CATHETER SYSTEM, MODEL 02200; REFORM PERIPHERAL CATHETERCATHETER, MODEL 02406

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024243
510(k) Type
Traditional
Applicant
Fox Hollow Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2003
Days to Decision
179 days
Submission Type
Summary

REFORM PERIPHERAL CATHETER SYSTEM, MODEL 02200; REFORM PERIPHERAL CATHETERCATHETER, MODEL 02406

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024243
510(k) Type
Traditional
Applicant
Fox Hollow Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2003
Days to Decision
179 days
Submission Type
Summary