The following data is part of a premarket notification filed by Imm Enterprises Ltd. with the FDA for Jakobi Surg. Instruments #7 10/43.
Device ID | K834188 |
510k Number | K834188 |
Device Name: | JAKOBI SURG. INSTRUMENTS #7 10/43 |
Classification | Hook, Microsurgical Ear |
Applicant | IMM ENTERPRISES LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JYL |
CFR Regulation Number | 874.4420 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-11-21 |
Decision Date | 1984-03-06 |