The following data is part of a premarket notification filed by Central Media with the FDA for Specialty Media.
| Device ID | K873259 |
| 510k Number | K873259 |
| Device Name: | SPECIALTY MEDIA |
| Classification | Culture Media, Selective And Differential |
| Applicant | CENTRAL MEDIA 10386 ROCKINGHAM DR. Sacramento, CA 95827 |
| Contact | Rebecca Clark |
| Correspondent | Rebecca Clark CENTRAL MEDIA 10386 ROCKINGHAM DR. Sacramento, CA 95827 |
| Product Code | JSI |
| CFR Regulation Number | 866.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-11 |
| Decision Date | 1987-11-06 |