510(k) K110120

ECHELON RAPID CARDIAC COIL by Hitachi Medical Systems America, Inc. — Product Code MOS

K110120 is an FDA 510(k) premarket notification submitted by Hitachi Medical Systems America, Inc. for the device "ECHELON RAPID CARDIAC COIL". The FDA issued a decision of Substantially Equivalent on February 25, 2011. The device falls under product code MOS (Coil, Magnetic Resonance, Specialty), a Class II device regulated under 21 CFR 892.1000. Hitachi Medical Systems America, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 25, 2011
Date Received
January 18, 2011
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