FDA 510(k) Application Details - K870035

Device Classification Name Alizarin Sulfonate, Calcium

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510(K) Number K870035
Device Name Alizarin Sulfonate, Calcium
Applicant EASTMAN KODAK COMPANY
343 STATE ST.
ROCHESTER, NY US
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Contact NORMAN H GEIL
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Regulation Number 862.1145

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Classification Product Code CID
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Date Received 01/05/1987
Decision Date 05/12/1987
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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