Luxatemp Automix
by DMG Chemisch-Pharmazeutische Fabrik GmbH
510(k) K924830
Luxatemp Automix is a Class II device made by DMG Chemisch-Pharmazeutische Fabrik GmbH, cleared under FDA 510(k) K924830 on 29 Apr 1994, 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 | NumberK924830 | Date29 Apr 1994 | StatusActive |
Official records
- FDA 510(k) database K924830
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EBG
- FDA applicant
- Dmg Chemisch Pharmazeutische Fabrik GmbH
- Device class
- Class II
- Regulation
- 21 CFR Part 872.3770
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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