The following data is part of a premarket notification filed by Degussa Corp. with the FDA for Degubond X-lite.
Device ID | K955027 |
510k Number | K955027 |
Device Name: | DEGUBOND X-LITE |
Classification | Alloy, Gold-based Noble Metal |
Applicant | DEGUSSA CORP. 3950 SOUTH CLINTON AVE. South Plainfield, NJ 07080 |
Contact | H. Meinicke |
Correspondent | H. Meinicke DEGUSSA CORP. 3950 SOUTH CLINTON AVE. South Plainfield, NJ 07080 |
Product Code | EJT |
CFR Regulation Number | 872.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-11-02 |
Decision Date | 1995-12-01 |