510(k) K231647

XENOVIEW 3.0T Chest Coil by Polarean, Inc. — Product Code MOS

K231647 is an FDA 510(k) premarket notification submitted by Polarean, Inc. for the device "XENOVIEW 3.0T Chest Coil". The FDA issued a decision of Substantially Equivalent on June 29, 2023. The device falls under product code MOS (Coil, Magnetic Resonance, Specialty), a Class II device regulated under 21 CFR 892.1000. Polarean, Inc. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 29, 2023
Date Received
June 5, 2023
Clearance Type
Special
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