Oxiplex— 510(k) K253326
Substantially EquivalentFziomed, Inc.
FDA 510(k) clearance K253326 for Oxiplex, Substantially Equivalent on 2026-05-01. 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
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Luis Obispo, CA, US
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