K891781 is an FDA 510(k) clearance for the TOXO ELISA TEST SYSTEM. This device is classified as a Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii (Class II - Special Controls, product code LGD).
Submitted by Zeus Scientific, Inc. (Raritan, US). The FDA issued a Cleared decision on July 14, 1989, 112 days after receiving the submission on March 24, 1989.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3780.
| 510(k) Number | K891781 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 24, 1989 |
| Decision Date | July 14, 1989 |
| Days to Decision | 112 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | LGD — Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.3780 |