K231801
- 510(k) number
- K231801
- Device name
- MedHealth DVT compression Devices MHH900S/MHH900E
- Applicant
- Medhealth Medical Limited CN
- Product code
- JOW — Sleeve, Limb, Compressible
- Decision date
- 2023-12-14
- Date received
- 2023-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K231801.pdf
Official FDA record: K231801
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.