Geneva— 510(k) K201272
Substantially EquivalentNucletron B.V.
FDA 510(k) clearance K201272 for Geneva, Substantially Equivalent on 2020-07-16. Applicant: Nucletron B.V.. Device class: 2.
Clearance details
- Applicant
- Nucletron B.V.
- Product code
- Code JAQ
- Device class
- Class 2
- Regulation
- 21 CFR 892.5700
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Veenendaal, NL
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