The following data is part of a premarket notification filed by Microline Scientific with the FDA for Differential Culture Med. Mannitol Salt.
| Device ID | K841841 |
| 510k Number | K841841 |
| Device Name: | DIFFERENTIAL CULTURE MED. MANNITOL SALT |
| Classification | Culture Media, Selective And Differential |
| Applicant | MICROLINE SCIENTIFIC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JSI |
| CFR Regulation Number | 866.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-04-17 |
| Decision Date | 1984-05-25 |