Oxiplex®— 510(k) DEN240038
UnknownFziomed, Inc.
FDA 510(k) clearance DEN240038 for Oxiplex®, Unknown on 2025-06-17. Applicant: Fziomed, Inc.. Device class: 2.
Clearance details
- Applicant
- Fziomed, Inc.
- Product code
- Product code QVL
- Device class
- Class 2
- Regulation
- 21 CFR 888.3047
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- San Luis Obispo, CA, US
Recent devices under product code QVL
view allMore clearances from Fziomed, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.