Browse hierarchy: [Immunology (IM)](/submissions/IM) → [Subpart F — Immunological Test Systems](/submissions/IM/subpart-f%E2%80%94immunological-test-systems) → [21 CFR 866.5700](/submissions/IM/subpart-f%E2%80%94immunological-test-systems/866.5700) → DGQ — Whole Blood Plasma, Antigen, Antiserum, Control

# DGQ · Whole Blood Plasma, Antigen, Antiserum, Control

_Immunology · 21 CFR 866.5700 · Class 1_

**Canonical URL:** https://fda.innolitics.com/submissions/IM/subpart-f%E2%80%94immunological-test-systems/DGQ

## Overview

- **Product Code:** DGQ
- **Device Name:** Whole Blood Plasma, Antigen, Antiserum, Control
- **Regulation:** [21 CFR 866.5700](/submissions/IM/subpart-f%E2%80%94immunological-test-systems/866.5700)
- **Device Class:** 1
- **Review Panel:** [Immunology](/submissions/IM)

## Identification

A whole human plasma or serum immunological test system is a device that consists of reagents used to measure by immunochemical techniques the proteins in plasma or serum. Measurements of proteins in plasma or serum aid in the diagnosis of any disease concerned with abnormal levels of plasma or serum proteins, e.g., agammaglobulinemia, allergies, multiple myeloma, rheumatoid vasculitis, or hereditary angioneurotic edema.

## Classification Rationale

Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 866.9.

## Recent Cleared Devices (1 of 1)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [K791282](https://fda.innolitics.com/submissions/IM/subpart-f%E2%80%94immunological-test-systems/DGQ/K791282.md) | ANTI-HUMAN SERUM | Diagnostica, Inc. | Oct 17, 1979 | SESE |

## Top Applicants

- Diagnostica, Inc. — 1 clearance

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**Source:** [https://fda.innolitics.com/submissions/IM/subpart-f%E2%80%94immunological-test-systems/DGQ](https://fda.innolitics.com/submissions/IM/subpart-f%E2%80%94immunological-test-systems/DGQ)

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