Parsortix PC1 Device— 510(k) DEN200062
UnknownAngle Europe , Ltd.
FDA 510(k) clearance DEN200062 for Parsortix PC1 Device, Unknown on 2022-05-24. Applicant: Angle Europe , Ltd..
Clearance details
- Applicant
- Angle Europe , Ltd.
- Product code
- Code QSA
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Guildford, GB
Data sourced from openFDA. This site is unofficial and independent of the FDA.