← Product Code [KNK](/submissions/CH/subpart-b%E2%80%94clinical-chemistry-test-systems/KNK) · K841702

# TDX REA URIC ACID (K841702)

_Abbott Laboratories · KNK · May 31, 1984 · Clinical Chemistry · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/CH/subpart-b%E2%80%94clinical-chemistry-test-systems/KNK/K841702

## Device Facts

- **Applicant:** Abbott Laboratories
- **Product Code:** [KNK](/submissions/CH/subpart-b%E2%80%94clinical-chemistry-test-systems/KNK.md)
- **Decision Date:** May 31, 1984
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 862.1775
- **Device Class:** Class 1
- **Review Panel:** Clinical Chemistry

## Regulatory Identification

A uric acid test system is a device intended to measure uric acid in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of numerous renal and metabolic disorders, including renal failure, gout, leukemia, psoriasis, starvation or other wasting conditions, and of patients receiving cytotoxic drugs.

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**Source:** [https://fda.innolitics.com/submissions/CH/subpart-b%E2%80%94clinical-chemistry-test-systems/KNK/K841702](https://fda.innolitics.com/submissions/CH/subpart-b%E2%80%94clinical-chemistry-test-systems/KNK/K841702)

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