Last synced on 14 November 2025 at 11:06 pm

Retrace Ureteral Access Sheath (ASXL10, ASXL12, ACXL10, ACXL12, AXXL10, AXXL12, ALXL10, ALXL12)

Page Type
Cleared 510(K)
510(k) Number
K242173
510(k) Type
Traditional
Applicant
Coloplast Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/2024
Days to Decision
111 days
Submission Type
Summary

Retrace Ureteral Access Sheath (ASXL10, ASXL12, ACXL10, ACXL12, AXXL10, AXXL12, ALXL10, ALXL12)

Page Type
Cleared 510(K)
510(k) Number
K242173
510(k) Type
Traditional
Applicant
Coloplast Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/2024
Days to Decision
111 days
Submission Type
Summary