← Product Code [HLQ](/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HLQ) · K944616

# KERATRON CORNEAL TOPOGRAPHER (K944616)

_Alliance Medical Marketinig · HLQ · Nov 22, 1994 · Ophthalmic · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HLQ/K944616

## Device Facts

- **Applicant:** Alliance Medical Marketinig
- **Product Code:** [HLQ](/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HLQ.md)
- **Decision Date:** Nov 22, 1994
- **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.

---

**Source:** [https://fda.innolitics.com/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HLQ/K944616](https://fda.innolitics.com/submissions/OP/subpart-b%E2%80%94diagnostic-devices/HLQ/K944616)

**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
