← Product Code [HLQ](/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HLQ) · K922253

# KERATOREF L60 (K922253)

_Luneau Ophtalmologie SA · HLQ · Jun 19, 1992 · Ophthalmic · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HLQ/K922253

## Device Facts

- **Applicant:** Luneau Ophtalmologie SA
- **Product Code:** [HLQ](/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HLQ.md)
- **Decision Date:** Jun 19, 1992
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 886.1350
- **Device Class:** Class 1
- **Review Panel:** Ophthalmic

## Regulatory Identification

A keratoscope is an AC-powered or battery-powered device intended to measure and evaluate the corneal curvature of the eye. Lines and circles within the keratoscope are used to observe the corneal reflex. This generic type of device includes the photokeratoscope which records corneal curvature by taking photographs of the cornea.

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**Source:** [https://fda.innolitics.com/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HLQ/K922253](https://fda.innolitics.com/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HLQ/K922253)

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