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Cytosponge Cell Collection Device

Page Type
Cleared 510(K)
510(k) Number
K181020
510(k) Type
Traditional
Applicant
Covidien llc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2018
Days to Decision
121 days
Submission Type
Summary

Cytosponge Cell Collection Device

Page Type
Cleared 510(K)
510(k) Number
K181020
510(k) Type
Traditional
Applicant
Covidien llc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2018
Days to Decision
121 days
Submission Type
Summary