The following data is part of a premarket notification filed by Microline Scientific with the FDA for Differential Culture Med. Levine Emb.
Device ID | K841843 |
510k Number | K841843 |
Device Name: | DIFFERENTIAL CULTURE MED. LEVINE EMB |
Classification | Culture Media, Non-selective And Differential |
Applicant | MICROLINE SCIENTIFIC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JSH |
CFR Regulation Number | 866.2320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-04-17 |
Decision Date | 1984-05-31 |