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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name High Intensity Ultrasound System For Prostate Tissue Ablation
510(k) Number K230692
Device Name TULSA-PRO System
Applicant
Profound Medical, Inc.
2400 Skymark Ave.
Unit 6
Mississauga,  CA L4W 5K5
Applicant Contact Nicole Baker
Correspondent
Profound Medical, Inc.
2400 Skymark Ave.
Unit 6
Mississauga,  CA L4W 5K5
Correspondent Contact Imen Ferchichi
Regulation Number876.4340
Classification Product Code
PLP  
Date Received03/13/2023
Decision Date 09/20/2023
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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