K163521 is an FDA 510(k) clearance for the Lumipulse G LH 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 January 12, 2017, 28 days after receiving the submission on December 15, 2016.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1150.
| 510(k) Number | K163521 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 15, 2016 |
| Decision Date | January 12, 2017 |
| Days to Decision | 28 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 |