Last synced on 25 January 2026 at 3:41 am

XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242003
510(k) Type
Traditional
Applicant
Aesculap, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2024
Days to Decision
160 days
Submission Type
Summary

XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242003
510(k) Type
Traditional
Applicant
Aesculap, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2024
Days to Decision
160 days
Submission Type
Summary