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EkoSonic Endovascular Device with Control Unit 4.0

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183361
510(k) Type
Traditional
Applicant
Btg International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2019
Days to Decision
122 days
Submission Type
Summary

EkoSonic Endovascular Device with Control Unit 4.0

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183361
510(k) Type
Traditional
Applicant
Btg International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2019
Days to Decision
122 days
Submission Type
Summary