Browse hierarchy: [Immunology (IM)](/submissions/IM) → [Subpart F — Immunological Test Systems](/submissions/IM/subpart-f%E2%80%94immunological-test-systems) → [21 CFR 866.5210](/submissions/IM/subpart-f%E2%80%94immunological-test-systems/866.5210) → JFQ — P-Phenyl-Enediamine/Edta (Spectrophotometric), Ceruloplasmin

# JFQ · P-Phenyl-Enediamine/Edta (Spectrophotometric), Ceruloplasmin

_Immunology · 21 CFR 866.5210 · Class 2_

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

## Overview

- **Product Code:** JFQ
- **Device Name:** P-Phenyl-Enediamine/Edta (Spectrophotometric), Ceruloplasmin
- **Regulation:** [21 CFR 866.5210](/submissions/IM/subpart-f%E2%80%94immunological-test-systems/866.5210)
- **Device Class:** 2
- **Review Panel:** [Immunology](/submissions/IM)

## Identification

A ceruloplasmin immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the ceruloplasmin (copper-transporting serum protein) in serum, other body fluids, or tissues. Measurements of ceruloplasmin aid in the diagnosis of copper metabolism disorders.

## Classification Rationale

Class II (special 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.

## Special Controls

*Classification.* Class II (special 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 (0 of 0)

_No cleared devices on record._

---

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

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com
