510(k) K212864

dS TorsoCardiac 1.5T, dS MSK S 1.5T, dS MSK M 1.5T by Philips Healthcare (Suzhou) Co., Ltd. — Product Code MOS

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 1, 2021
Date Received
September 8, 2021
Clearance Type
Traditional
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