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pRESET LITE Thrombectomy Device

Page Type
Cleared 510(K)
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)
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