The following data is part of a premarket notification filed by Isle Media And Sterile Products, Inc. with the FDA for Xld Agar (xylase Lysine Desoxy Agar).
Device ID | K791477 |
510k Number | K791477 |
Device Name: | XLD AGAR (XYLASE LYSINE DESOXY AGAR) |
Classification | Culture Media, Selective And Differential |
Applicant | ISLE MEDIA AND STERILE PRODUCTS, INC. 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 | 1979-07-30 |
Decision Date | 1979-09-04 |