K243229
- 510(k) number
- K243229
- Device name
- Bunkerhill AVC
- Applicant
- BunkerHill Health CA · US
- Product code
- JAK — System, X-Ray, Tomography, Computed
- Decision date
- 2025-01-27
- Date received
- 2024-10-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.1 MB · U.S. public domain
Also available from FDA: K243229.pdf
Official FDA record: K243229
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.