Last synced on 30 September 2022 at 11:05 pm

LIGHT GUIDE CABLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111342
510(k) Type
Traditional
Applicant
SCHOTT NORTH AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2011
Days to Decision
196 days
Submission Type
Summary

LIGHT GUIDE CABLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111342
510(k) Type
Traditional
Applicant
SCHOTT NORTH AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2011
Days to Decision
196 days
Submission Type
Summary