K110641 is an FDA 510(k) clearance for the FUJIREBIO DIAGNOSTICS VITAMIN D CONTROL. This device is classified as a Single (specified) Analyte Controls (assayed And Unassayed) (Class I - General Controls, product code JJX).
Submitted by Fujirebio Diagnostics,Inc. (Seguin, US). The FDA issued a Cleared decision on May 27, 2011, 84 days after receiving the submission on March 4, 2011.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1660.
| 510(k) Number | K110641 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 04, 2011 |
| Decision Date | May 27, 2011 |
| Days to Decision | 84 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | JJX — Single (specified) Analyte Controls (assayed And Unassayed) |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1660 |