The following data is part of a premarket notification filed by Kulzer, Inc. with the FDA for Translux Cl.
| Device ID | K843823 |
| 510k Number | K843823 |
| Device Name: | TRANSLUX CL |
| Classification | Activator, Ultraviolet, For Polymerization |
| Applicant | KULZER, INC. 111 N. WABASH AVE. Chicago, IL 60602 |
| Contact | Robert W Bauer |
| Correspondent | Robert W Bauer KULZER, INC. 111 N. WABASH AVE. Chicago, IL 60602 |
| Product Code | EBZ |
| CFR Regulation Number | 872.6070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-09-28 |
| Decision Date | 1984-12-04 |