K914388 is an FDA 510(k) clearance for the C1 RID KIT. This device is classified as a Complement C1q, Antigen, Antiserum, Control (Class II - Special Controls, product code DAK).
Submitted by The Binding Site, Ltd. (Los Angeles, US). The FDA issued a Cleared decision on October 28, 1991, 27 days after receiving the submission on October 1, 1991.
This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5240.
| 510(k) Number | K914388 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 01, 1991 |
| Decision Date | October 28, 1991 |
| Days to Decision | 27 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Statement |
| Product Code | DAK — Complement C1q, Antigen, Antiserum, Control |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.5240 |