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 |