SuniIQ Digital Radiography System— 510(k) K162585
Substantially EquivalentSuni Medical Imaging, Inc.
FDA 510(k) clearance K162585 for SuniIQ Digital Radiography System, Substantially Equivalent on 2016-11-04. Applicant: Suni Medical Imaging, Inc.. Device class: 2.
Clearance details
- Applicant
- Suni Medical Imaging, Inc.
- Product code
- Code MUH
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Jose, CA, US
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