The following data is part of a premarket notification filed by Granite Diagnostics, Inc. with the FDA for Martin Lewis Transgrow.
| Device ID | K771872 |
| 510k Number | K771872 |
| Device Name: | MARTIN LEWIS TRANSGROW |
| Classification | Culture Media, For Isolation Of Pathogenic Neisseria |
| Applicant | GRANITE DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JTY |
| CFR Regulation Number | 866.2410 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-10-04 |
| Decision Date | 1977-10-25 |