FDA 510(k) Application Details - K070532

Device Classification Name Set, Administration, Intravascular

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510(K) Number K070532
Device Name Set, Administration, Intravascular
Applicant ICU MEDICAL, INC
4455 ATHERTON DR.
SALT LAKE CITY, UT 84123 US
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Contact MARTIN MAIER
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Regulation Number 880.5440

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Classification Product Code FPA
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Date Received 02/26/2007
Decision Date 03/20/2007
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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