UltraScan 650— 510(k) K161919
Substantially EquivalentCyberlogic, Inc.
FDA 510(k) clearance K161919 for UltraScan 650, Substantially Equivalent on 2017-04-05. Applicant: Cyberlogic, Inc.. Device class: 2.
Clearance details
- Applicant
- Cyberlogic, Inc.
- Product code
- Code MUA
- Device class
- Class 2
- Regulation
- 21 CFR 892.1180
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Recent devices under product code MUA
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