CerroZone Mini— 510(k) K242102
Substantially EquivalentCerrozone, LLC
FDA 510(k) clearance K242102 for CerroZone Mini, Substantially Equivalent on 2024-11-19. Applicant: Cerrozone, LLC. Device class: 2.
Clearance details
- Applicant
- Cerrozone, LLC
- Product code
- Code FRF
- Device class
- Class 2
- Regulation
- 21 CFR 880.5045
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Maryland Heights, MO, US
Recent devices under product code FRF
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