FDA 510(k) Application Details - K061492

Device Classification Name Syringe, Piston

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510(K) Number K061492
Device Name Syringe, Piston
Applicant TYCO HEALTHCARE
15 HAMPSHIRE ST.
MANSFIELD, MA 02048 US
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Contact MICHELLE KELLEY
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Regulation Number 880.5860

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Classification Product Code FMF
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Date Received 05/31/2006
Decision Date 08/03/2006
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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