Aurolloyd KF
FDA 510(k) K983080 · Bego U.S.A.
510(k) numberK983080
Submission
- Device name
- Aurolloyd KF
- Applicant
- Bego U.S.A.
Pawtucket, RI, US - Received
- September 2, 1998
- Decision date
- October 28, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Other 510(k)s with product code EJT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K052463 | Prometal HN86EJT · Traditional | Prometal Technologies | 10/14/2005SE |
| K041378 | Bio 60EJT · Traditional | Kodent, Inc. | 08/02/2004SE |
| K040672 | Porta ReflexEJT · Traditional | Wieland Dental + Technik GmbH & Co. KG | 05/27/2004SE |
| K040524 | Porta Solder 1090 WEJT · Traditional | Wieland Dental + Technik GmbH & Co. KG | 05/20/2004SE |
| K040043 | NDX-40 AlloyEJT · Traditional | Heraeus Kulzer, Inc. | 03/03/2004SE |
| K034049 | Herador Ec, PF, C, H, NH, G, GG and MP; Heraloy U and G; Herabond N; Albabond C, B and…EJT · Traditional | Heraeus Kulzer,GmbH | 03/01/2004SE |
| K033279 | Gold Dental Casting AlloysEJT · Traditional | Bego U.S.A. | 01/15/2004SE |
| K033446 | APEX93, APEX87, APEX84, APEX85, APEX77, E-Sarang 88 and E-Sarang 82EJT · Traditional | We Dong Myung Dental Industrial Co., Ltd. | 11/13/2003SE |
| K033435 | E-Sarang 86, DM78, DM55EJT · Traditional | We Dong Myung Dental Industrial Co., Ltd. | 11/12/2003SE |
| K032320 | Appollo 3 AlloyEJT · Traditional | Dentsply International | 10/01/2003SE |
More from Dentsply International
| 510(k) | Device | Decision |
|---|---|---|
| K033279 | Gold Dental Casting AlloysEJT · Traditional | 01/15/2004SE |
| K032136 | Wirobond CEJH · Traditional | 09/04/2003SE |
| K983082 | Begocer GEJT · Traditional | 10/28/1998SE |
| K983079 | Platinlloyd 100EJT · Traditional | 10/23/1998SE |
| K983078 | BegopalEJS · Traditional | 10/23/1998SE |
| K983077 | Bio PontostarEJT · Traditional | 10/23/1998SE |
Questions and answers
When was Aurolloyd KF cleared by the FDA?
Aurolloyd KF (K983080) received a 510(k) decision of Substantially Equivalent on October 28, 1998, 56 days after the submission was received.
What is the product code of K983080?
The FDA product code is EJT – Alloy, Gold-Based Noble Metal, a Class II (moderate risk) device regulated under 21 CFR 872.3060.