Browse hierarchy: [Ophthalmic (OP)](/submissions/OP) → [Subpart B — Diagnostic Devices](/submissions/OP/subpart-b%E2%80%94diagnostic-devices) → [21 CFR 886.1860](/submissions/OP/subpart-b%E2%80%94diagnostic-devices/886.1860) → HRE — Cabinet, Instrument, Ac-Powered, Ophthalmic

# HRE · Cabinet, Instrument, Ac-Powered, Ophthalmic

_Ophthalmic · 21 CFR 886.1860 · Class 1_

**Canonical URL:** https://fda.innolitics.com/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HRE

## Overview

- **Product Code:** HRE
- **Device Name:** Cabinet, Instrument, Ac-Powered, Ophthalmic
- **Regulation:** [21 CFR 886.1860](/submissions/OP/subpart-b%E2%80%94diagnostic-devices/886.1860)
- **Device Class:** 1
- **Review Panel:** [Ophthalmic](/submissions/OP)

## Identification

An ophthalmic instrument stand is an AC-powered or nonpowered device intended to store ophthalmic instruments in a readily accessible position.

## Classification Rationale

Class I (general controls). The AC-powered device and the battery-powered device are exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in § 886.9. The battery-powered device is also exempt from the current good manufacturing practice requirements of the quality management system regulation in part 820 of this chapter, except for requirements concerning records and complaint files under § 820.35 of this chapter.

## Recent Cleared Devices (0 of 0)

_No cleared devices on record._

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**Source:** [https://fda.innolitics.com/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HRE](https://fda.innolitics.com/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HRE)

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