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Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave E8 Peripheral IVL Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240225
510(k) Type
Traditional
Applicant
Shockwave Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2024
Days to Decision
56 days
Submission Type
Summary

Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave E8 Peripheral IVL Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240225
510(k) Type
Traditional
Applicant
Shockwave Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2024
Days to Decision
56 days
Submission Type
Summary