# Analyzer, Medical Image
> **Product code: MYN** · Class II — Moderate Risk (510(k) clearance required) · Radiology · 21 CFR 892.2070
## Classification
- **FDA Product Code:** MYN
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 892.2070
- **Review panel:** RA
- **Medical specialty:** Radiology
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Definition

For information on the MYN device, please see:  https://www.federalregister.gov/documents/2020/01/22/2020-00494/radiology-devices-reclassification-of-medical-image-analyzers

## Market data
- **Cleared 510(k) submissions:** 36
- **Registered establishments:** 28
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=MYN)
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