Submission Details
| 510(k) Number | K132227 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 17, 2013 |
| Decision Date | October 25, 2013 |
| Days to Decision | 100 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
K132227 is an FDA 510(k) clearance for the LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-TRILEVEL, LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-LEVEL I, LIQUICHEK IMMUNOASSAY, a Multi-analyte Controls, All Kinds (assayed) (Class I — General Controls, product code JJY), submitted by Bio-Rad Laboratories (Irvine, US). The FDA issued a Cleared decision on October 25, 2013, 100 days after receiving the submission on July 17, 2013. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1660.
| 510(k) Number | K132227 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 17, 2013 |
| Decision Date | October 25, 2013 |
| Days to Decision | 100 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | JJY — Multi-analyte Controls, All Kinds (assayed) |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 862.1660 |