LIGMAJECT
Syringe, Cartridge
ALAN J. KHEDARRI D.D.S., INC.
The following data is part of a premarket notification filed by Alan J. Khedarri D.d.s., Inc. with the FDA for Ligmaject.
Pre-market Notification Details
| Device ID | K802483 |
| 510k Number | K802483 |
| Device Name: | LIGMAJECT |
| Classification | Syringe, Cartridge |
| Applicant | ALAN J. KHEDARRI D.D.S., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EJI |
| CFR Regulation Number | 872.6770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-10-09 |
| Decision Date | 1980-11-12 |
Trademark Results [LIGMAJECT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LIGMAJECT 79092871 4062044 Live/Registered |
Henke-Sass Wolf GmbH 2010-12-13 |
 LIGMAJECT 73295772 1186570 Dead/Cancelled |
Ligmaject Produktionsgesellschaft fur medizinische Gerate mbH 1981-02-05 |
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