Transit-Pellets— 510(k) K222000
Substantially EquivalentMedifactia AB
FDA 510(k) clearance K222000 for Transit-Pellets, Substantially Equivalent on 2023-01-18. Applicant: Medifactia AB. Device class: 2.
Clearance details
- Applicant
- Medifactia AB
- Product code
- Code FFX
- Device class
- Class 2
- Regulation
- 21 CFR 876.1725
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stockholm, SE
Recent devices under product code FFX
view allMore clearances from Medifactia AB
view allAdverse events under product code FFX
product code FFX- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.