ViMove
by Dorsavi Ltd
510(k) K142494
ViMove is a Class II device made by Dorsavi Ltd, cleared under FDA 510(k) K142494 on 28 May 2015, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK142494 | Date28 May 2015 | StatusActive |
Official records
- FDA 510(k) database K142494
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- IKN
- FDA applicant
- Dorsavi, Ltd.
- Device class
- Class II
- Regulation
- 21 CFR Part 890.1375
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
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