FDA 510(k) Application Details - K955129

Device Classification Name Conserver, Oxygen

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510(K) Number K955129
Device Name Conserver, Oxygen
Applicant EAGLE MEDICAL EQUIPMENT CO.
3134 W. LEWIS #30
PHX, AZ 85017 US
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Contact LAWRENCE PELLERITO
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Regulation Number 868.5905

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Classification Product Code NFB
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Date Received 11/09/1995
Decision Date 02/16/1996
Decision SESE - SUBST EQUIV
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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