Fist Assist Devices Model FA-1— 510(k) K210281
Substantially EquivalentFist Assist Devices, LLC
FDA 510(k) clearance K210281 for Fist Assist Devices Model FA-1, Substantially Equivalent on 2021-06-17. Applicant: Fist Assist Devices, LLC.
Clearance details
- Applicant
- Fist Assist Devices, LLC
- Product code
- Code IRP
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Los Altos, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.