K223228
- 510(k) number
- K223228
- Device name
- Dayspring
- Applicant
- Koya Medical, Inc. CA · US
- Product code
- JOW — Sleeve, Limb, Compressible
- Decision date
- 2024-01-04
- Date received
- 2022-10-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K223228.pdf
Official FDA record: K223228
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.