PEACH 2, PEACH 2 Duo, PEACH 2 go— 510(k) K231977
Substantially EquivalentForeo, Inc.
FDA 510(k) clearance K231977 for PEACH 2, PEACH 2 Duo, PEACH 2 go, Substantially Equivalent on 2023-09-25. Applicant: Foreo, Inc.. Device class: 2.
Clearance details
- Applicant
- Foreo, Inc.
- Product code
- Code OHT
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Las Vegas, NV, US
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More clearances from Foreo, Inc.
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