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KSEA ROTOCUT G1 ELECTROMECHANICAL MORCELLATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061180
510(k) Type
Traditional
Applicant
KARL STORZ ENDOSCOPY-AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/2006
Days to Decision
91 days
Submission Type
Summary