FDA 510(k) Application Details - K903103

Device Classification Name Acid, Phosphoric-Tungstic (Spectrophotometric), Chloride

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510(K) Number K903103
Device Name Acid, Phosphoric-Tungstic (Spectrophotometric), Chloride
Applicant SYNERMED, INC.
1688 50TH AVENUE,
MONTREAL (LACHINE),
QUEBEC, CANADA H8T 2V5 CA
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Contact MARCIA J ARENTZ
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Regulation Number 862.1170

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Classification Product Code CHG
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Date Received 07/13/1990
Decision Date 08/09/1990
Decision SE - Substantially Equivalent
Classification Advisory Committee CH - Clinical Chemistry
Review Advisory Committee CH - Clinical Chemistry
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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