FDA 510(k) Application Details - K090469

Device Classification Name Camera, Multi Format, Radiological

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510(K) Number K090469
Device Name Camera, Multi Format, Radiological
Applicant CARESTREAM HEALTH, INC.
1 IMATION WAY
304-4B-28
OAKDALE, MN 55128-3414 US
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Contact GAYLE CARROLL
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Regulation Number 892.2040

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Classification Product Code LMC
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Date Received 02/23/2009
Decision Date 05/22/2009
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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