Last synced on 14 November 2025 at 11:06 pm

pRESET Delta Thrombectomy Device and pRESET Delta LITE Thrombectomy Device

Page Type
Cleared 510(K)
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)
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