Eroxon— 510(k) DEN220078
UnknownFutura Medical Developments Limited
FDA 510(k) clearance DEN220078 for Eroxon, Unknown on 2023-06-09. Applicant: Futura Medical Developments Limited. Device class: 2.
Clearance details
- Applicant
- Futura Medical Developments Limited
- Product code
- Code QWW
- Device class
- Class 2
- Regulation
- 21 CFR 876.5021
- Advisory panel
- Gastroenterology, Urology
- 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.