K242102
- 510(k) number
- K242102
- Device name
- CerroZone Mini
- Applicant
- Cerrozone, LLC MO · US
- Product code
- FRF — Cleaner, Air, Medical Recirculating
- Decision date
- 2024-11-19
- Date received
- 2024-07-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242102.pdf
Official FDA record: K242102
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.