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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Cystometer, Electrical Recording
510(k) Number K253537
Device Name Glean Urodynamics System Male Delivery System (GUS-1000-M); Glean Urodynamics System Female Delivery System (GUS-1000-F); Glean Urodynamics System Uroflowmeter (UFM-1000 (Uroflowmeter)); Glean Urodynamics System Abdominal Sensor (GUS-1000-A)
Applicant
Bright Uro, Inc.
3 Goddard
Irvine,  CA  92618
Applicant Contact Suranjan Roychowdhury
Correspondent
Bright Uro, Inc.
3 Goddard
Irvine,  CA  92618
Correspondent Contact Suranjan Roychowdhury
Regulation Number876.1620
Classification Product Code
EXQ  
Subsequent Product Code
EXY  
Date Received11/13/2025
Decision Date 04/16/2026
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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