FDA 510(k) Application Details - K003840

Device Classification Name Apparatus, Exhaust, Surgical

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510(K) Number K003840
Device Name Apparatus, Exhaust, Surgical
Applicant I.C. MEDICAL, INC.
2002 W. QUAIL AVE.
PHOENIX, AZ 85027-2610 US
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Contact CRAIG HARSHMAN
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Regulation Number 878.5070

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Classification Product Code FYD
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Date Received 12/12/2000
Decision Date 02/01/2001
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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