Flowflex® Plus COVID-19 Home Test— 510(k) K233373
Substantially EquivalentACON Laboratories, Inc.
FDA 510(k) clearance K233373 for Flowflex® Plus COVID-19 Home Test, Substantially Equivalent on 2024-04-19. Applicant: ACON Laboratories, Inc..
Clearance details
- Applicant
- ACON Laboratories, Inc.
- Product code
- Code QYT
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.