FDA 510(k) Applications Submitted by Kristine Canavan

FDA 510(k) Number	Submission Date	Device Name	Applicant
K231279	05/03/2023	Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mm	Ablative Solutions, Inc.
K001741	06/08/2000	RADIONICS RF DISC CATHETER ELECTRODE SYSTEM	RADIONICS, INC.
K032307	07/25/2003	CAP BONE SUBSTITUTE MATERIAL	ETEX CORP.