FAQ 101— 510(k) K222012
Substantially EquivalentForeo, Inc.
FDA 510(k) clearance K222012 for FAQ 101, Substantially Equivalent on 2023-04-05. 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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