Last synced on 25 January 2026 at 3:41 am

pRESET LITE Thrombectomy Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231539
510(k) Type
Traditional
Applicant
Phenox Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
10/21/2023
Days to Decision
144 days
Submission Type
Summary

pRESET LITE Thrombectomy Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231539
510(k) Type
Traditional
Applicant
Phenox Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
10/21/2023
Days to Decision
144 days
Submission Type
Summary