Last synced on 25 January 2026 at 3:41 am

ProdiGI

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN220006
510(k) Type
Direct
Applicant
Covidien, LLC
Country
United States
FDA Decision
Deleted
Decision Date
6/13/2022
Days to Decision
150 days

ProdiGI

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN220006
510(k) Type
Direct
Applicant
Covidien, LLC
Country
United States
FDA Decision
Deleted
Decision Date
6/13/2022
Days to Decision
150 days