Usi Basic. AG 1050. AG 1090
510(k) K873146
Usi Basic. AG 1050. AG 1090 is a Class II device made by Cranston Ind., Inc., cleared under FDA 510(k) K873146 on 27 Oct 1987, 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 | NumberK873146 | Date27 Oct 1987 | StatusActive |
Official records
- FDA 510(k) database K873146
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ELC
- Device class
- Class II
- Regulation
- 21 CFR Part 872.4850
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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