The following data is part of a premarket notification filed by Acumedia Manufacturers, Inc. with the FDA for Lowenstein-jensen Medium Base.
Device ID | K833220 |
510k Number | K833220 |
Device Name: | LOWENSTEIN-JENSEN MEDIUM BASE |
Classification | Culture Media, Selective And Non-differential |
Applicant | ACUMEDIA MANUFACTURERS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JSJ |
CFR Regulation Number | 866.2360 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-09-19 |
Decision Date | 1983-10-27 |