Zytron
by Premier Dental Products Co.
510(k) K780796
Zytron is a Class II device made by Premier Dental Products Co., cleared under FDA 510(k) K780796 on 22 Jun 1978, 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 | NumberK780796 | Date22 Jun 1978 | StatusActive |
Official records
- FDA 510(k) database K780796
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EBF
- Device class
- Class II
- Regulation
- 21 CFR Part 872.3690
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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