INTRALIG
Syringe, Cartridge
MILTEX INSTRUMENT CO.
The following data is part of a premarket notification filed by Miltex Instrument Co. with the FDA for Intralig.
Pre-market Notification Details
| Device ID | K823536 |
| 510k Number | K823536 |
| Device Name: | INTRALIG |
| Classification | Syringe, Cartridge |
| Applicant | MILTEX INSTRUMENT CO. 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 | 1982-11-30 |
| Decision Date | 1982-12-28 |
Trademark Results [INTRALIG]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INTRALIG 73405239 not registered Dead/Abandoned |
E. MILTENBERG, INC. 1982-12-08 |
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