DVT Motion Pneumatic Compression Device— 510(k) K232270
Substantially EquivalentKoge Micro Tech Co., Ltd.
FDA 510(k) clearance K232270 for DVT Motion Pneumatic Compression Device, Substantially Equivalent on 2024-03-06. Applicant: Koge Micro Tech Co., Ltd..
Clearance details
- Applicant
- Koge Micro Tech Co., Ltd.
- Product code
- Code JOW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New Taipei, TW
Data sourced from openFDA. This site is unofficial and independent of the FDA.