FDA 510(k) Application Details - K931873

Device Classification Name Arterial Blood Sampling Kit

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510(K) Number K931873
Device Name Arterial Blood Sampling Kit
Applicant STEVEN FRANK MERCEREAU
4911 WEST LAKE DR.
CONYERS, GA US
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Contact STEVEN F MERCEREAU
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Regulation Number 868.1100

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Classification Product Code CBT
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Date Received 04/14/1993
Decision Date 12/30/1993
Decision KD - Substantially Equivalent - Kit with Drugs
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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