K012291 is an FDA 510(k) clearance for the HUMAN IGG SUBCLASS LIQUID REAGENT KITS, PRODUCT CODE LK001.TA. This device is classified as a Method, Nephelometric, Immunoglobulins (g, A, M) (Class II - Special Controls, product code CFN).
Submitted by The Binding Site, Ltd. (Santa Monica, US). The FDA issued a Cleared decision on August 20, 2001, 31 days after receiving the submission on July 20, 2001.
This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5510.
| 510(k) Number | K012291 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 20, 2001 |
| Decision Date | August 20, 2001 |
| Days to Decision | 31 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Statement |
| Product Code | CFN — Method, Nephelometric, Immunoglobulins (g, A, M) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.5510 |