← Product Code [KJI](/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/KJI) · K782125

# RIA KIT, KANAMYCIN (K782125)

_Diagnostic Products Corp. · KJI · Jan 10, 1979 · Clinical Toxicology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/KJI/K782125

## Device Facts

- **Applicant:** Diagnostic Products Corp.
- **Product Code:** [KJI](/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/KJI.md)
- **Decision Date:** Jan 10, 1979
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 862.3520
- **Device Class:** Class 2
- **Review Panel:** Clinical Toxicology

## Regulatory Identification

A kanamycin test system is a device intended to measure kanamycin, an antibiotic drug, in plasma and serum. Measurements obtained by this device are used in the diagnosis and treatment of kanamycin overdose and in monitoring levels of kanamycin to ensure appropriate therapy.

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**Source:** [https://fda.innolitics.com/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/KJI/K782125](https://fda.innolitics.com/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/KJI/K782125)

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