K252471
- 510(k) number
- K252471
- Device name
- Paptizer 360
- Applicant
- LiViliti Health Products Corporation FL · US
- Product code
- QXQ — Respiratory Accessory Microbial Reduction Device.
- Decision date
- 2026-04-29
- Date received
- 2025-08-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K252471.pdf
Official FDA record: K252471
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.