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PowerWire Radiofrequency Guidewire Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232562
510(k) Type
Traditional
Applicant
Baylis Medical Technologies Inc.
Country
Canada
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/28/2024
Days to Decision
188 days
Submission Type
Summary

PowerWire Radiofrequency Guidewire Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232562
510(k) Type
Traditional
Applicant
Baylis Medical Technologies Inc.
Country
Canada
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/28/2024
Days to Decision
188 days
Submission Type
Summary