K880679 is an FDA 510(k) clearance for the BION CMV-G TEST SYSTEM. This device is classified as a Antigen, Cf (including Cf Control), Cytomegalovirus (Class II - Special Controls, product code GQH).
Submitted by Bion Ent., Ltd. (Park Ridge, US). The FDA issued a Cleared decision on June 3, 1988, 105 days after receiving the submission on February 19, 1988.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3175.
| 510(k) Number | K880679 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 19, 1988 |
| Decision Date | June 03, 1988 |
| Days to Decision | 105 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | GQH — Antigen, Cf (including Cf Control), Cytomegalovirus |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.3175 |