← Product Code [IXH](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IXH) · K851811

# SLIT CAMERA MODEL 07-624 (K851811)

_Victoreen, Inc. · IXH · May 28, 1985 · Radiology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IXH/K851811

## Device Facts

- **Applicant:** Victoreen, Inc.
- **Product Code:** [IXH](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IXH.md)
- **Decision Date:** May 28, 1985
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 892.1940
- **Device Class:** Class 1
- **Review Panel:** Radiology

## Regulatory Identification

A radiologic quality assurance instrument is a device intended for medical purposes to measure a physical characteristic associated with another radiologic device.

---

**Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IXH/K851811](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IXH/K851811)

**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
