The following data is part of a premarket notification filed by Micro Media Laboratories with the FDA for Sim Medium.
| Device ID | K834012 |
| 510k Number | K834012 |
| Device Name: | SIM MEDIUM |
| Classification | Culture Media, Multiple Biochemical Test |
| Applicant | MICRO MEDIA LABORATORIES 803 N. Front St. Suite 3 McHenry, IL 60050 |
| Product Code | JSE |
| CFR Regulation Number | 866.2320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-21 |
| Decision Date | 1983-12-22 |