FAQ (102)— 510(k) K240616
Substantially EquivalentForeo, Inc.
FDA 510(k) clearance K240616 for FAQ (102), Substantially Equivalent on 2024-07-15. Applicant: Foreo, Inc.. Device class: 2.
Clearance details
- Applicant
- Foreo, Inc.
- Product code
- Code PAY
- Device class
- Class 2
- Regulation
- 21 CFR 878.4420
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Las Vegas, NV, US
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