FDA 510(k) Application Details - K983314

Device Classification Name Injector, Contrast Medium, Automatic

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510(K) Number K983314
Device Name Injector, Contrast Medium, Automatic
Applicant NYCOMED AMERSHAM IMAGING
49 PLAIN ST.
NORTH ATTLEBORO, MA 02760 US
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Contact ROSINA ROBINSON
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Regulation Number 870.1650

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Classification Product Code IZQ
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Date Received 09/21/1998
Decision Date 02/19/1999
Decision SESE - SUBST EQUIV
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee CV - Cardiovascular
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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