Last synced on 25 January 2026 at 3:41 am

MODIFICATION TO AUTOCON II 400 ELECTROSURGICAL GENERATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062464
510(k) Type
Traditional
Applicant
Karl Storz Endoscopy-America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/2007
Days to Decision
176 days
Submission Type
Summary

MODIFICATION TO AUTOCON II 400 ELECTROSURGICAL GENERATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062464
510(k) Type
Traditional
Applicant
Karl Storz Endoscopy-America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/2007
Days to Decision
176 days
Submission Type
Summary