FDA 510(k) Application Details - K832933

Device Classification Name Mercury, Atomic Absorption

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510(K) Number K832933
Device Name Mercury, Atomic Absorption
Applicant JEROME INSTRUMENT CORP.


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Regulation Number 862.3600

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Classification Product Code DPH
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Date Received 08/30/1983
Decision Date 11/25/1983
Decision SE - Substantially Equivalent
Classification Advisory Committee CH - Clinical Chemistry
Review Advisory Committee TX - Clinical Toxicology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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