Myocene— 510(k) DEN230051

Unknown

Myocene

FDA 510(k) clearance DEN230051 for Myocene, Unknown on 2025-01-17. Applicant: Myocene.

Clearance details

Applicant: Myocene
Product code: Code SDX
Advisory panel: Neurology
Date received: 2023-07-27
Decision date: 2025-01-17
Decision: Unknown
Clearance type: Direct
Location: Liège, BE

View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.