FDA 510(k) Application Details - K801833

Device Classification Name Column Supports, Glc

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510(K) Number K801833
Device Name Column Supports, Glc
Applicant SUPELCO, INC.


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Regulation Number 862.2250

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Classification Product Code DJA
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Date Received 08/01/1980
Decision Date 08/27/1980
Decision SE - Substantially Equivalent
Classification Advisory Committee TX - Clinical Toxicology
Review Advisory Committee CH - Clinical Chemistry
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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