K163053 is an FDA 510(k) clearance for the Lumipulse G E2-III Calibrators. This device is classified as a Calibrator, Secondary (Class II - Special Controls, product code JIT).
Submitted by Fujirebio Diagnostics,Inc. (Malvern, US). The FDA issued a Cleared decision on December 1, 2016, 30 days after receiving the submission on November 1, 2016.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1150.
| 510(k) Number | K163053 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 01, 2016 |
| Decision Date | December 01, 2016 |
| Days to Decision | 30 days |
| Submission Type | Abbreviated |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | JIT — Calibrator, Secondary |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1150 |