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FLEX ENDOSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
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)
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