Last synced on 6 December 2024 at 11:05 pm

CEREGLIDE 92 Catheter System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233982
510(k) Type
Special
Applicant
Cerenovus Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2024
Days to Decision
143 days
Submission Type
Summary

CEREGLIDE 92 Catheter System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233982
510(k) Type
Special
Applicant
Cerenovus Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2024
Days to Decision
143 days
Submission Type
Summary