K812313 is an FDA 510(k) clearance for the SANDARE URIC ACID PROCEDURE. This device is classified as a Acid, Uric, Acid Reduction Of Ferric Ion (Class I - General Controls, product code LFQ).
Submitted by Sandare Chemical Co., Inc. (Mchenry, US). The FDA issued a Cleared decision on September 1, 1981, 15 days after receiving the submission on August 17, 1981.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1775.
| 510(k) Number | K812313 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 17, 1981 |
| Decision Date | September 01, 1981 |
| Days to Decision | 15 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | LFQ — Acid, Uric, Acid Reduction Of Ferric Ion |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1775 |