510(k) K241069

iLoop Interventional Coil 0.55T by Noras Mri Products GmbH — Product Code MOS

K241069 is an FDA 510(k) premarket notification submitted by Noras Mri Products GmbH for the device "iLoop Interventional Coil 0.55T". The FDA issued a decision of Substantially Equivalent on June 7, 2024. The device falls under product code MOS (Coil, Magnetic Resonance, Specialty), a Class II device regulated under 21 CFR 892.1000. Noras Mri Products GmbH has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 7, 2024
Date Received
April 19, 2024
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Coil, Magnetic Resonance, Specialty
Device Class
Class II
Regulation Number
892.1000
Review Panel
RA
Submission Type