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
- 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
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