Last synced on 25 January 2026 at 3:41 am

RUDOLF INNOVIEW AUTOCLAVABLE SEMI-RIGID URETERO-RENOSCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062707
510(k) Type
Traditional
Applicant
Innovative Endoscopy Components, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2006
Days to Decision
88 days
Submission Type
Summary

RUDOLF INNOVIEW AUTOCLAVABLE SEMI-RIGID URETERO-RENOSCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062707
510(k) Type
Traditional
Applicant
Innovative Endoscopy Components, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2006
Days to Decision
88 days
Submission Type
Summary