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PrecisePath™ Radiofrequency Puncture Generator and PrecisePath™ Footswitch

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250275
510(k) Type
Traditional
Applicant
Baylis Medical Technologies, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/28/2025
Days to Decision
270 days
Submission Type
Summary

PrecisePath™ Radiofrequency Puncture Generator and PrecisePath™ Footswitch

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250275
510(k) Type
Traditional
Applicant
Baylis Medical Technologies, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/28/2025
Days to Decision
270 days
Submission Type
Summary