K232300
- 510(k) number
- K232300
- Device name
- ElastiMed SACS
- Applicant
- Elastimed , Ltd. IL
- Product code
- JOW — Sleeve, Limb, Compressible
- Decision date
- 2023-12-22
- Date received
- 2023-08-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K232300.pdf
Official FDA record: K232300
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.