510(k) K242096

dS FootAnkle Coil 8ch 1.5T by Philips Medical Systems Nederland B.V. — Product Code MOS

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 12, 2024
Date Received
July 18, 2024
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