The following data is part of a premarket notification filed by Imm Enterprises Ltd. with the FDA for Jakobi Surg. Instruments #3 21/22/24.
| Device ID | K834192 |
| 510k Number | K834192 |
| Device Name: | JAKOBI SURG. INSTRUMENTS #3 21/22/24 |
| Classification | Surgical Instruments, G-u, Manual (and Accessories) |
| Applicant | IMM ENTERPRISES LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KOA |
| CFR Regulation Number | 876.4730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-21 |
| Decision Date | 1984-03-22 |