FDA 510(k) Application Details - K872718

Device Classification Name Flowmeter, Tube, Thorpe, Back-Pressure Compensated

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510(K) Number K872718
Device Name Flowmeter, Tube, Thorpe, Back-Pressure Compensated
Applicant PURITAN BENNETT CORP.
9401 INDIAN CREEK PKWY.
P.O. BOX 25905
OVERLAND PARK, KS US
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Contact HARTLEY C ERICSON
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Regulation Number 868.2340

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Classification Product Code CAX
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Date Received 07/10/1987
Decision Date 08/05/1987
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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