FDA 510(k) Application Details - K903939

Device Classification Name Analyzer, Gas, Helium, Gaseous-Phase

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510(K) Number K903939
Device Name Analyzer, Gas, Helium, Gaseous-Phase
Applicant MEDICAL ASSOCIATED SERVICES, INC.
P.O. BOX 530
HATFIELD, PA US
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Contact MARK S ALSBERGE
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Regulation Number 868.1640

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Classification Product Code BSE
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Date Received 08/27/1990
Decision Date 01/03/1991
Decision SE - Substantially Equivalent
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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