K091910 is an FDA 510(k) clearance for the PICCOLO MAGNESIUM TEST SYSTEM. This device is classified as a Photometric Method, Magnesium (Class I - General Controls, product code JGJ).
Submitted by Abaxis, Inc. (Union City, US). The FDA issued a Cleared decision on October 1, 2009, 98 days after receiving the submission on June 25, 2009.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1495.
| 510(k) Number | K091910 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 25, 2009 |
| Decision Date | October 01, 2009 |
| Days to Decision | 98 days |
| Submission Type | Special |
| Review Panel | Chemistry (CH) |
| Summary | Statement |
| Product Code | JGJ — Photometric Method, Magnesium |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1495 |