Cytosponge Cell Collection Device— 510(k) K181020
Substantially EquivalentCovidien, LLC
FDA 510(k) clearance K181020 for Cytosponge Cell Collection Device, Substantially Equivalent on 2018-08-16. Applicant: Covidien, LLC.
Clearance details
- Applicant
- Covidien, LLC
- Product code
- Code EOX
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mansfield, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.