The following data is part of a premarket notification filed by Degussa Ag with the FDA for Duceranium U.
| Device ID | K926347 |
| 510k Number | K926347 |
| Device Name: | DUCERANIUM U |
| Classification | Alloy, Metal, Base |
| Applicant | DEGUSSA AG 3950 SOUTH CLINTON AVE. South Plainfield, NJ 07080 |
| Contact | Holger Meinicke |
| Correspondent | Holger Meinicke DEGUSSA AG 3950 SOUTH CLINTON AVE. South Plainfield, NJ 07080 |
| Product Code | EJH |
| CFR Regulation Number | 872.3710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-12-17 |
| Decision Date | 1993-05-27 |