Last synced on 14 November 2025 at 11:06 pm

REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETER

Page Type
Cleared 510(K)
510(k) Number
K110076
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2011
Days to Decision
219 days
Submission Type
Summary

REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETER

Page Type
Cleared 510(K)
510(k) Number
K110076
510(k) Type
Traditional
Applicant
STERILMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2011
Days to Decision
219 days
Submission Type
Summary