FDA 510(k) Application Details - K073180

Device Classification Name Counter, Sponge, Surgical

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510(K) Number K073180
Device Name Counter, Sponge, Surgical
Applicant CLEARCOUNT MEDICAL SOLUTIONS, INC.
101 BELLEVUE ROAD
SUITE 300
PITTSBURGH, PA 15229 US
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Contact JEFF WOLFGONG
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Regulation Number 880.2740

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Classification Product Code LWH
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Date Received 11/13/2007
Decision Date 11/19/2007
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party Y
Expedited Review



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