Last synced on 5 July 2024 at 11:05 pm

EMBOGUARD Balloon Guide Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233924
510(k) Type
Special
Applicant
Neuravi Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
4/18/2024
Days to Decision
127 days
Submission Type
Summary

EMBOGUARD Balloon Guide Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233924
510(k) Type
Special
Applicant
Neuravi Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
4/18/2024
Days to Decision
127 days
Submission Type
Summary