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PowerWire® 14 Radiofrequency Guidewire Kit

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251158
510(k) Type
Traditional
Applicant
Baylis Medical Technologies, Inc.
Country
Canada
FDA Decision
Substantially Equivalent - Kit
Decision Date
9/11/2025
Days to Decision
149 days
Submission Type
Summary

PowerWire® 14 Radiofrequency Guidewire Kit

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251158
510(k) Type
Traditional
Applicant
Baylis Medical Technologies, Inc.
Country
Canada
FDA Decision
Substantially Equivalent - Kit
Decision Date
9/11/2025
Days to Decision
149 days
Submission Type
Summary