K232270
- 510(k) number
- K232270
- Device name
- DVT Motion Pneumatic Compression Device
- Applicant
- Koge Micro Tech Co., Ltd. TW
- Product code
- JOW — Sleeve, Limb, Compressible
- Decision date
- 2024-03-06
- Date received
- 2023-07-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K232270.pdf
Official FDA record: K232270
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.