The following data is part of a premarket notification filed by Micro Media Laboratories with the FDA for Mod Thayer Martin Martin Lewis.
| Device ID | K850841 |
| 510k Number | K850841 |
| Device Name: | MOD THAYER MARTIN MARTIN LEWIS |
| Classification | Culture Media, For Isolation Of Pathogenic Neisseria |
| Applicant | MICRO MEDIA LABORATORIES 2775 KURTZ SAN DIEGO, CA 92110 |
| Contact | PETER G MARTIN |
| Correspondent | PETER G MARTIN MICRO MEDIA LABORATORIES 2775 KURTZ SAN DIEGO, CA 92110 |
| Product Code | JTY |
| CFR Regulation Number | 866.2410 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-03-01 |
| Decision Date | 1985-03-20 |