Utah Artifical Arm
510(k) K802642
Utah Artifical Arm is a Class I device made by Motion Control, Inc., cleared under FDA 510(k) K802642 on 12 Nov 1980, active as of 12 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 | NumberK802642 | Date12 Nov 1980 | StatusActive |
Official records
- FDA 510(k) database K802642
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- IRE
- Device class
- Class I
- Regulation
- 21 CFR Part 890.3420
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code IRE (Joint, Elbow, External Limb Component, Powered).