The following data is part of a premarket notification filed by Imm Enterprises Ltd. with the FDA for H.r. Jakobi Surg. Instruments #4 30/31.
| Device ID | K834177 |
| 510k Number | K834177 |
| Device Name: | H.R. JAKOBI SURG. INSTRUMENTS #4 30/31 |
| Classification | Amniotome |
| Applicant | IMM ENTERPRISES LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HGE |
| CFR Regulation Number | 884.4530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-21 |
| Decision Date | 1983-12-27 |