K963084 is an FDA 510(k) clearance for the OPUS CMV TEST SYSTEM-MODIFICATION. This device is classified as a Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus (Class II - Special Controls, product code LFZ).
Submitted by Behring Diagnostics, Inc. (Westwood, US). The FDA issued a Cleared decision on October 9, 1996, 62 days after receiving the submission on August 8, 1996.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3175.
| 510(k) Number | K963084 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 08, 1996 |
| Decision Date | October 09, 1996 |
| Days to Decision | 62 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Summary PDF |
| Product Code | LFZ — Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.3175 |