SYRINGE
Syringe, Piston
I M, INC.
The following data is part of a premarket notification filed by I M, Inc. with the FDA for Syringe.
Pre-market Notification Details
| Device ID | K833399 |
| 510k Number | K833399 |
| Device Name: | SYRINGE |
| Classification | Syringe, Piston |
| Applicant | I M, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-05 |
| Decision Date | 1984-01-10 |
Trademark Results [SYRINGE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SYRINGE 76266839 2525156 Live/Registered |
J.R. SIMPLOT COMPANY 2001-06-05 |
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