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CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800822
510(k) Type
Traditional
Applicant
KLI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1980
Days to Decision
64 days

CO2 CYSTOSCOPY/URETHROSCOPY CONSOLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800822
510(k) Type
Traditional
Applicant
KLI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1980
Days to Decision
64 days