Koios DS— 510(k) K242130
Substantially EquivalentKoios Medical, Inc.
FDA 510(k) clearance K242130 for Koios DS, Substantially Equivalent on 2024-11-15. Applicant: Koios Medical, Inc..
Clearance details
- Applicant
- Koios Medical, Inc.
- Product code
- Code POK
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.