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Metacross RX PTA Balloon Dilitation Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150865
510(k) Type
Traditional
Applicant
KANEKA Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/3/2015
Days to Decision
124 days
Submission Type
Summary

Metacross RX PTA Balloon Dilitation Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150865
510(k) Type
Traditional
Applicant
KANEKA Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/3/2015
Days to Decision
124 days
Submission Type
Summary