Carony
by Bruno Independent Living Aids, Inc.
510(k) K002205
Carony is a medical device (FDA Class I; FDA product code IOR, Wheelchair, Mechanical) made by Bruno Independent Living Aids, Inc., cleared under FDA 510(k) K002205 on 10 Aug 2000, 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 | NumberK002205 | Date10 Aug 2000 | StatusActive |
Official records
- FDA 510(k) database K002205
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- IOR
- Device class
- Class I
- Regulation
- 21 CFR Part 890.3850
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
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