Oxiplex®— 510(k) DEN240038

Unknown

Fziomed, Inc.

FDA 510(k) clearance DEN240038 for Oxiplex®, Unknown on 2025-06-17. Applicant: Fziomed, Inc..

Clearance details

Applicant: Fziomed, Inc.
Product code: Code QVL
Advisory panel: Orthopedic
Date received: 2024-07-22
Decision date: 2025-06-17
Decision: Unknown
Clearance type: Direct
Location: San Luis Obispo, CA, US

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