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FLEX ENDOSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140662
510(k) Type
Traditional
Applicant
Design Standards Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2014
Days to Decision
89 days
Submission Type
Summary

FLEX ENDOSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140662
510(k) Type
Traditional
Applicant
Design Standards Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2014
Days to Decision
89 days
Submission Type
Summary