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MODULITH LITHOTRIPSY, MODEL SLK FOR THE FRAGMENTATION OF URINARY AND UPPER URETERAL CALCULI

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010340
510(k) Type
Traditional
Applicant
Karl Storz Lithotripsy-America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2001
Days to Decision
8 days
Submission Type
Summary

MODULITH LITHOTRIPSY, MODEL SLK FOR THE FRAGMENTATION OF URINARY AND UPPER URETERAL CALCULI

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010340
510(k) Type
Traditional
Applicant
Karl Storz Lithotripsy-America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2001
Days to Decision
8 days
Submission Type
Summary