Air Compression Therapy Device— 510(k) K201694
Substantially EquivalentShenzhen Dongjilian Electronics Co., Ltd.
FDA 510(k) clearance K201694 for Air Compression Therapy Device, Substantially Equivalent on 2020-11-19. Applicant: Shenzhen Dongjilian Electronics Co., Ltd..
Clearance details
- Applicant
- Shenzhen Dongjilian Electronics Co., Ltd.
- Product code
- Code IRP
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.