K003671 is an FDA 510(k) clearance for the LAMBDA IMMAGE FREELITE KIT. This device is classified as a Lambda, Antigen, Antiserum, Control (Class II - Special Controls, product code DEH).
Submitted by The Binding Site, Ltd. (Santa Monica, US). The FDA issued a Cleared decision on February 1, 2001, 65 days after receiving the submission on November 28, 2000.
This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5550.
| 510(k) Number | K003671 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 28, 2000 |
| Decision Date | February 01, 2001 |
| Days to Decision | 65 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Statement |
| Product Code | DEH — Lambda, Antigen, Antiserum, Control |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.5550 |