Stryker Leg Exerciser
510(k) K831910
Stryker Leg Exerciser is a Class I device made by Stryker Corp., cleared under FDA 510(k) K831910 on 12 Jul 1983, 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 | NumberK831910 | Date12 Jul 1983 | StatusActive |
Official records
- FDA 510(k) database K831910
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- BXB
- Device class
- Class I
- Regulation
- 21 CFR Part 890.5380
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
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