K103603 is an FDA 510(k) clearance for the ZEUS ELISA HSV GG-2 IGG TEST SYSTEM. This device is classified as a Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-2 (Class II - Special Controls, product code MYF).
Submitted by Zeus Scientific, Inc. (Branchburg, US). The FDA issued a Cleared decision on May 20, 2011, 163 days after receiving the submission on December 8, 2010.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3305.
| 510(k) Number | K103603 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 08, 2010 |
| Decision Date | May 20, 2011 |
| Days to Decision | 163 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Statement |
| Product Code | MYF — Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-2 |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.3305 |