EOS— 510(k) K120721
Substantially EquivalentEos Imaging
FDA 510(k) clearance K120721 for EOS, Substantially Equivalent on 2012-04-06. Applicant: Eos Imaging. Device class: 2.
Clearance details
- Applicant
- Eos Imaging
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Washington, DC, US
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