LED PHOTIC System— 510(k) K211974
Substantially EquivalentMicromed S.P.A.
FDA 510(k) clearance K211974 for LED PHOTIC System, Substantially Equivalent on 2021-09-23. Applicant: Micromed S.P.A.. Device class: 2.
Clearance details
- Applicant
- Micromed S.P.A.
- Product code
- Code GWE
- Device class
- Class 2
- Regulation
- 21 CFR 882.1890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mogliano Veneto, IT
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