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FDA 510(k) Application Details - K091047
Device Classification Name
Coil, Magnetic Resonance, Specialty
More FDA Info for this Device
510(K) Number
K091047
Device Name
Coil, Magnetic Resonance, Specialty
Applicant
LMT MEDICAL SYSTEMS GMBH
OSTERWEIDE 8
LUEBECK 23562 DE
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Contact
KRISTINA LUETJE
Other 510(k) Applications for this Contact
Regulation Number
892.1000
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Classification Product Code
MOS
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More FDA Info for this Product Code
Date Received
04/13/2009
Decision Date
08/18/2010
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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