The following data is part of a premarket notification filed by Unitek Corp. with the FDA for Concerto.
Device ID | K831097 |
510k Number | K831097 |
Device Name: | CONCERTO |
Classification | Alloy, Other Noble Metal |
Applicant | UNITEK CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | EJS |
CFR Regulation Number | 872.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-04-04 |
Decision Date | 1983-06-15 |