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Excipio LV Thrombectomy Device

Page Type
Cleared 510(K)
510(k) Number
K223897
510(k) Type
Traditional
Applicant
Contego Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2023
Days to Decision
51 days
Submission Type
Summary

Excipio LV Thrombectomy Device

Page Type
Cleared 510(K)
510(k) Number
K223897
510(k) Type
Traditional
Applicant
Contego Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2023
Days to Decision
51 days
Submission Type
Summary