Edge Digital Flat Panel X-ray Detector— 510(k) K172682
Substantially EquivalentOsko, Inc.
FDA 510(k) clearance K172682 for Edge Digital Flat Panel X-ray Detector, Substantially Equivalent on 2017-10-06. Applicant: Osko, Inc..
Clearance details
- Applicant
- Osko, Inc.
- Product code
- Code MQB
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.