Wand Plus
510(k) K992819
Wand Plus is a Class II device made by Spintech, Inc., cleared under FDA 510(k) K992819 on 11 May 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 | NumberK992819 | Date11 May 2000 | StatusActive |
Official records
- FDA 510(k) database K992819
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EJI
- Device class
- Class II
- Regulation
- 21 CFR Part 872.6770
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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- ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE by ARNOLD TUBER INDUSTRIES