K242295
- 510(k) number
- K242295
- Device name
- BunkerHill BMD
- Applicant
- BunkerHill Health CA · US
- Product code
- KGI — Densitometer, Bone
- Decision date
- 2025-04-08
- Date received
- 2024-08-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K242295.pdf
Official FDA record: K242295
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.