Browse hierarchy: [Radiology (RA)](/submissions/RA) → [Subpart B — Diagnostic Devices](/submissions/RA/subpart-b%E2%80%94diagnostic-devices) → [21 CFR 892.2050](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/892.2050) → QQE — Image Management Software For Planning Of Otologic And Neurotologic Procedures

# QQE · Image Management Software For Planning Of Otologic And Neurotologic Procedures

_Radiology · 21 CFR 892.2050 · Class 2_

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

## Overview

- **Product Code:** QQE
- **Device Name:** Image Management Software For Planning Of Otologic And Neurotologic Procedures
- **Regulation:** [21 CFR 892.2050](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/892.2050)
- **Device Class:** 2
- **Review Panel:** [Radiology](/submissions/RA)

## Identification

A medical image management and processing system is a device that provides one or more capabilities relating to the review and digital processing of medical images for the purposes of interpretation by a trained practitioner of disease detection, diagnosis, or patient management. The software components may provide advanced or complex image processing functions for image manipulation, enhancement, or quantification that are intended for use in the interpretation and analysis of medical images. Advanced image manipulation functions may include image segmentation, multimodality image registration, or 3D visualization. Complex quantitative functions may include semi-automated measurements or time-series measurements.

## Classification Rationale

Class II (special controls; voluntary standards—Digital Imaging and Communications in Medicine (DICOM) Std., Joint Photographic Experts Group (JPEG) Std., Society of Motion Picture and Television Engineers (SMPTE) Test Pattern).

## Special Controls

*Classification.* Class II (special controls; voluntary standards—Digital Imaging and Communications in Medicine (DICOM) Std., Joint Photographic Experts Group (JPEG) Std., Society of Motion Picture and Television Engineers (SMPTE) Test Pattern).

## Recent Cleared Devices (3 of 3)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [K242120](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/QQE/K242120.md) | OTOPLAN | Cascination AG | Apr 11, 2025 | SESE |
| [K220300](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/QQE/K220300.md) | OTOPLAN | Cascination AG | Jun 24, 2022 | SESE |
| [K203486](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/QQE/K203486.md) | Otoplan | Cascination AG | Aug 20, 2021 | SESE |

## Top Applicants

- Cascination AG — 3 clearances

---

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

**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