iLoop Interventional Coil 0.55T— 510(k) K241069
Substantially EquivalentNoras Mri Products GmbH
FDA 510(k) clearance K241069 for iLoop Interventional Coil 0.55T, Substantially Equivalent on 2024-06-07. Applicant: Noras Mri Products GmbH. Device class: 2.
Clearance details
- Applicant
- Noras Mri Products GmbH
- Product code
- Code MOS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1000
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Höchberg, DE
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Data sourced from openFDA. This site is unofficial and independent of the FDA.