FDA 510(k) Applications Submitted by Baylis Medical Technologies Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K230571 03/01/2023 RFP-100A Connector Cable (Single Use) Baylis Medical Technologies Inc.
K232562 08/24/2023 PowerWire Radiofrequency Guidewire Kit Baylis Medical Technologies Inc.


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