K042092 is an FDA 510(k) clearance for the ATHENA MULTI-LYTE EBV VCA IGM TEST SYSTEM. This device is classified as a Antibody Igm, If, Epstein-barr Virus (Class I - General Controls, product code LJN).
Submitted by Zeus Scientific, Inc. (Raritan, US). The FDA issued a Cleared decision on April 12, 2005, 252 days after receiving the submission on August 3, 2004.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3235.
| 510(k) Number | K042092 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 03, 2004 |
| Decision Date | April 12, 2005 |
| Days to Decision | 252 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Statement |
| Product Code | LJN — Antibody Igm, If, Epstein-barr Virus |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.3235 |