FDA 510(k) Application Details - K822288

Device Classification Name Radioimmunoassay, Luteinizing Hormone

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510(K) Number K822288
Device Name Radioimmunoassay, Luteinizing Hormone
Applicant CORNING MEDICAL & SCIENTIFIC

, US
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Regulation Number 862.1485

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Classification Product Code CEP
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Date Received 07/30/1982
Decision Date 09/13/1982
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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