FAQ (302)— 510(k) K242747
Substantially EquivalentForeo, Inc.
FDA 510(k) clearance K242747 for FAQ (302), Substantially Equivalent on 2024-12-11. Applicant: Foreo, Inc.. Device class: 2.
Clearance details
- Applicant
- Foreo, Inc.
- Product code
- Code OAP
- Device class
- Class 2
- Regulation
- 21 CFR 890.5500
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Las Vegas, NV, US
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