FDA 510(k) Application Details - K002899

Device Classification Name Powered Laser Surgical Instrument

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510(K) Number K002899
Device Name Powered Laser Surgical Instrument
Applicant OPUSDENT LTD.
117 AHUZAH ST.
RA'ANANNA IL
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Contact SHOSHANA FRIEDMAN
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Regulation Number 878.4810

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Classification Product Code GEX
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Date Received 09/18/2000
Decision Date 12/12/2000
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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