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Cytosponge Cell Collection Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152794
510(k) Type
Traditional
Applicant
Covidien LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2016
Days to Decision
197 days
Submission Type
Summary

Cytosponge Cell Collection Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152794
510(k) Type
Traditional
Applicant
Covidien LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2016
Days to Decision
197 days
Submission Type
Summary