Overlapped Compression Therapy
FDA 510(k) clearance K202839 · decided 2021-01-21
Clearance details
- K-number
- K202839
- Device name
- Overlapped Compression Therapy
- Applicant
- Jkh Health Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2020-09-25
- Decision date
- 2021-01-21
- Days to decision
- 118 days
- Clearance type
- Traditional
- Product code
- JOW
- Device class
- 2
- Regulation number
- 870.5800
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Shenzhen, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.