FDA 510(k) Application Details - K925175

Device Classification Name Table, Radiographic, Tilting

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510(K) Number K925175
Device Name Table, Radiographic, Tilting
Applicant SHIMADZU MEDICAL SYSTEMS
101 WEST WALNUT ST.
GARDENIA, CA US
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Contact DE MINT
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Regulation Number 892.1980

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Classification Product Code IXR
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Date Received 10/13/1992
Decision Date 11/27/1992
Decision SE - Substantially Equivalent
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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