FDA 510(k) Application Details - K101359

Device Classification Name Syringe, Piston

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510(K) Number K101359
Device Name Syringe, Piston
Applicant INVIRO MEDICAL DEVICES, INC.
1755 NORTH BROWN ROAD
SUITE 150
LAWRENCEVILLE, GA 30043 US
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Contact JIM BARLEY
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Regulation Number 880.5860

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Classification Product Code FMF
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Date Received 05/14/2010
Decision Date 08/20/2010
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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