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Ultravision2™ System Integrated Monopolar L-Hook (H/S)™

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231298
510(k) Type
Traditional
Applicant
Alesi Surgical Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/31/2023
Days to Decision
180 days
Submission Type
Summary

Ultravision2™ System Integrated Monopolar L-Hook (H/S)™

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231298
510(k) Type
Traditional
Applicant
Alesi Surgical Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/31/2023
Days to Decision
180 days
Submission Type
Summary