Last synced on 14 November 2025 at 11:06 pm

Prodeon Urethral Sheath System

Page Type
Cleared 510(K)
510(k) Number
K252572
510(k) Type
Traditional
Applicant
Prodeon Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2025
Days to Decision
54 days
Submission Type
Summary

Prodeon Urethral Sheath System

Page Type
Cleared 510(K)
510(k) Number
K252572
510(k) Type
Traditional
Applicant
Prodeon Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2025
Days to Decision
54 days
Submission Type
Summary