K240499
- 510(k) number
- K240499
- Device name
- ARTAIRA Arterial Compression Device (AACD01)
- Applicant
- Airos Medical, Inc. PA · US
- Product code
- JOW — Sleeve, Limb, Compressible
- Decision date
- 2024-10-11
- Date received
- 2024-02-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K240499.pdf
Official FDA record: K240499
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.