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Shock Pulse-SE Lithotripsy System CYBERWAND II

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142428
510(k) Type
Traditional
Applicant
Cybersonics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2014
Days to Decision
76 days
Submission Type
Summary

Shock Pulse-SE Lithotripsy System CYBERWAND II

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142428
510(k) Type
Traditional
Applicant
Cybersonics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2014
Days to Decision
76 days
Submission Type
Summary