The following data is part of a premarket notification filed by Zeus Scientific, Inc. with the FDA for Toxoplasma Antibody Test System.
| Device ID | K791571 |
| 510k Number | K791571 |
| Device Name: | TOXOPLASMA ANTIBODY TEST SYSTEM |
| Classification | Antigens, If, Toxoplasma Gondii |
| Applicant | ZEUS SCIENTIFIC, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GLZ |
| CFR Regulation Number | 866.3780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-08-13 |
| Decision Date | 1979-09-24 |