Parsortix PC1 Device— 510(k) DEN200062

Unknown

Angle 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
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Data sourced from openFDA. This site is unofficial and independent of the FDA.