FDA 510(k) Application Details - K042172

Device Classification Name Set, Administration, Intravascular

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510(K) Number K042172
Device Name Set, Administration, Intravascular
Applicant SMITHS MEDICAL MD, INC.
1265 GREY FOX ROAD
ST. PAUL, MN 55112 US
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Contact DAVID H SHORT
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Regulation Number 880.5440

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Classification Product Code FPA
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Date Received 08/11/2004
Decision Date 10/07/2004
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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