The following data is part of a premarket notification filed by Hardy Media with the FDA for Motility Indole Ornithine Agar.
| Device ID | K850547 |
| 510k Number | K850547 |
| Device Name: | MOTILITY INDOLE ORNITHINE AGAR |
| Classification | Culture Media, Multiple Biochemical Test |
| Applicant | HARDY MEDIA 205 W.MONTECITO ST. Santa Barbara, CA 93101 |
| Contact | Jay Hardy |
| Correspondent | Jay Hardy HARDY MEDIA 205 W.MONTECITO ST. Santa Barbara, CA 93101 |
| Product Code | JSE |
| CFR Regulation Number | 866.2320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-02-11 |
| Decision Date | 1985-03-11 |