← Product Code [GGT](/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/GGT) · K903492

# DSL ERYTHROPOIETIN (DSL # 1100) (K903492)

_Diagnostic Systems Laboratories, Inc. · GGT · Oct 26, 1990 · Hematology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/GGT/K903492

## Device Facts

- **Applicant:** Diagnostic Systems Laboratories, Inc.
- **Product Code:** [GGT](/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/GGT.md)
- **Decision Date:** Oct 26, 1990
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 864.7250
- **Device Class:** Class 2
- **Review Panel:** Hematology

## Regulatory Identification

A erythropoietin assay is a device that measures the concentration of erythropoietin (an enzyme that regulates the production of red blood cells) in serum or urine. This assay provides diagnostic information for the evaluation of erythrocytosis (increased total red cell mass) and anemia.

## Special Controls

*Classification.* Class II. The special control for this device is FDA's “Document for Special Controls for Erythropoietin Assay Premarket Notification (510(k)s).”

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**Source:** [https://fda.innolitics.com/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/GGT/K903492](https://fda.innolitics.com/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/GGT/K903492)

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