The following data is part of a premarket notification filed by Remel Co. with the FDA for Diamond's Medium Modified.
| Device ID | K881995 |
| 510k Number | K881995 |
| Device Name: | DIAMOND'S MEDIUM MODIFIED |
| Classification | Culture Media, Enriched |
| Applicant | REMEL CO. 12076 SANTA FE DR. Lenexa, KS 66215 |
| Contact | Brenda Henry |
| Correspondent | Brenda Henry REMEL CO. 12076 SANTA FE DR. Lenexa, KS 66215 |
| Product Code | KZI |
| CFR Regulation Number | 866.2330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-05-12 |
| Decision Date | 1988-06-02 |