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KSEA CLEARVISION II, MODEL 40334120

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072410
510(k) Type
Traditional
Applicant
KARL STORZ ENDOSCOPY-AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2008
Days to Decision
256 days
Submission Type
Summary

KSEA CLEARVISION II, MODEL 40334120

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072410
510(k) Type
Traditional
Applicant
KARL STORZ ENDOSCOPY-AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2008
Days to Decision
256 days
Submission Type
Summary