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ScopeSeal Duodenoscope Protective Device

Page Type
Cleared 510(K)
510(k) Number
K183171
510(k) Type
Traditional
Applicant
Gi Scientific, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2019
Days to Decision
326 days
Submission Type
Summary

ScopeSeal Duodenoscope Protective Device

Page Type
Cleared 510(K)
510(k) Number
K183171
510(k) Type
Traditional
Applicant
Gi Scientific, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2019
Days to Decision
326 days
Submission Type
Summary