EchoS Family— 510(k) K202514
Substantially EquivalentEcholight S.P.A
FDA 510(k) clearance K202514 for EchoS Family, Substantially Equivalent on 2021-02-25. Applicant: Echolight S.P.A. Device class: 2.
Clearance details
- Applicant
- Echolight S.P.A
- Product code
- Code MUA
- Device class
- Class 2
- Regulation
- 21 CFR 892.1180
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lecce, IT
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