K233441
- 510(k) number
- K233441
- Device name
- The Vest APX System (PVAPX1)
- Applicant
- Baxter Healthcare Corportation IL · US
- Product code
- BYI — Percussor, Powered-Electric
- Decision date
- 2024-03-22
- Date received
- 2023-10-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K233441.pdf
Official FDA record: K233441
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.