FDA 510(k) Application Details - K033099

Device Classification Name Set, Administration, Intravascular

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510(K) Number K033099
Device Name Set, Administration, Intravascular
Applicant APPLIED DIABETES RESEARCH, INCORPORATED
28481 LAFALDA
LAGUNA NIGUEL, CA 92677 US
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Contact JIM BARLEY
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Regulation Number 880.5440

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Classification Product Code FPA
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Date Received 09/29/2003
Decision Date 10/16/2003
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review



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