The following data is part of a premarket notification filed by Jeneric Ind. with the FDA for Rexillium Iii.
| Device ID | K833143 |
| 510k Number | K833143 |
| Device Name: | REXILLIUM III |
| Classification | Alloy, Metal, Base |
| Applicant | JENERIC IND. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | EJH |
| CFR Regulation Number | 872.3710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-15 |
| Decision Date | 1983-12-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() REXILLIUM III 73316665 1230790 Dead/Cancelled |
Jeneric Industries, Inc. 1981-06-29 |