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FDA 510(k) Application Details - K960359
Device Classification Name
Mixer, Breathing Gases, Anesthesia Inhalation
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510(K) Number
K960359
Device Name
Mixer, Breathing Gases, Anesthesia Inhalation
Applicant
HAMILTON MEDICAL, INC.
P.O. BOX 30008
RENO, NV 89520 US
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Contact
TIM COWART
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Regulation Number
868.5330
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Classification Product Code
BZR
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More FDA Info for this Product Code
Date Received
01/25/1996
Decision Date
04/24/1996
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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