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CEREGLIDE 92 Intermediate Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230726
510(k) Type
Traditional
Applicant
Cerenovus, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2023
Days to Decision
258 days
Submission Type
Summary

CEREGLIDE 92 Intermediate Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230726
510(k) Type
Traditional
Applicant
Cerenovus, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2023
Days to Decision
258 days
Submission Type
Summary