The following data is part of a premarket notification filed by Meridian Diagnostics, Inc. with the FDA for Negative Control Serum.
| Device ID | K792694 |
| 510k Number | K792694 |
| Device Name: | NEGATIVE CONTROL SERUM |
| Classification | Antiserum, Positive Control, Histoplasma Capsulatum |
| Applicant | MERIDIAN DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GMK |
| CFR Regulation Number | 866.3320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-12-27 |
| Decision Date | 1980-01-24 |