Browse hierarchy: [Microbiology (MI)](/submissions/MI) → [Subpart D — Serological Reagents](/submissions/MI/subpart-d%E2%80%94serological-reagents) → [21 CFR 866.3035](/submissions/MI/subpart-d%E2%80%94serological-reagents/866.3035) → GTE — Antisera, Arizona Spp., All

# GTE · Antisera, Arizona Spp., All

_Microbiology · 21 CFR 866.3035 · Class 1_

**Canonical URL:** https://fda.innolitics.com/submissions/MI/subpart-d%E2%80%94serological-reagents/GTE

## Overview

- **Product Code:** GTE
- **Device Name:** Antisera, Arizona Spp., All
- **Regulation:** [21 CFR 866.3035](/submissions/MI/subpart-d%E2%80%94serological-reagents/866.3035)
- **Device Class:** 1
- **Review Panel:** [Microbiology](/submissions/MI)

## Identification

Arizona spp. serological reagents are devices that consist of antisera and antigens used to identify Arizona spp. in cultured isolates derived from clinical specimens. The identification aids in the diagnosis of disease caused by bacteria belonging to the genus Arizona and provides epidemiological information on diseases caused by these microorganisms. Arizona spp. can cause gastroenteritis (food poisoning) and sepsis (blood poisoning).

## 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 (0 of 0)

_No cleared devices on record._

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**Source:** [https://fda.innolitics.com/submissions/MI/subpart-d%E2%80%94serological-reagents/GTE](https://fda.innolitics.com/submissions/MI/subpart-d%E2%80%94serological-reagents/GTE)

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