Last synced on 27 June 2025 at 11:06 pm

pRESET Delta Thrombectomy Device and pRESET Delta LITE Thrombectomy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242676
510(k) Type
Special
Applicant
phenox Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
2/28/2025
Days to Decision
175 days
Submission Type
Summary

pRESET Delta Thrombectomy Device and pRESET Delta LITE Thrombectomy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242676
510(k) Type
Special
Applicant
phenox Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
2/28/2025
Days to Decision
175 days
Submission Type
Summary