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Flexible HD Cysto-Urethroscope System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191357
510(k) Type
Traditional
Applicant
KARL STORZ Endoscopy-America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2019
Days to Decision
120 days
Submission Type
Summary

Flexible HD Cysto-Urethroscope System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191357
510(k) Type
Traditional
Applicant
KARL STORZ Endoscopy-America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2019
Days to Decision
120 days
Submission Type
Summary