The following data is part of a premarket notification filed by Isle Media And Sterile Products, Inc. with the FDA for Media For In-vitro Diagnostic Use.
| Device ID | K820863 |
| 510k Number | K820863 |
| Device Name: | MEDIA FOR IN-VITRO DIAGNOSTIC USE |
| Classification | Culture Media, Selective And Non-differential |
| Applicant | ISLE MEDIA AND STERILE PRODUCTS, 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 | 1982-03-29 |
| Decision Date | 1982-04-16 |