← Product Code [LFM](/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/LFM) · K942610

# KODAK EXTACHEM CLINICAL CHEMISTRY SLIDE DIGOXIN (DGXN) (K942610)

_Eastman Kodak Company · LFM · Oct 20, 1994 · Clinical Toxicology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/CH/subpart-d%E2%80%94clinical-toxicology-test-systems/LFM/K942610

## Device Facts

- **Applicant:** Eastman Kodak Company
- **Product Code:** [LFM](/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/LFM.md)
- **Decision Date:** Oct 20, 1994
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 862.3300
- **Device Class:** Class 2
- **Review Panel:** Clinical Toxicology

## Regulatory Identification

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

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**Source:** [https://fda.innolitics.com/submissions/CH/subpart-d%E2%80%94clinical-toxicology-test-systems/LFM/K942610](https://fda.innolitics.com/submissions/CH/subpart-d%E2%80%94clinical-toxicology-test-systems/LFM/K942610)

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