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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name flowmeter, tube, thorpe, back-pressure compensated
510(k) Number K872718
Device Name SERIES D FLOWMETER
Applicant
PURITAN BENNETT CORP.
9401 INDIAN CREEK PKWY.
P.O. BOX 25905
OVERLAND PARK,  KS  66225
Applicant Contact HARTLEY C ERICSON
Correspondent
PURITAN BENNETT CORP.
9401 INDIAN CREEK PKWY.
P.O. BOX 25905
OVERLAND PARK,  KS  66225
Correspondent Contact HARTLEY C ERICSON
Regulation Number868.2340
Classification Product Code
CAX  
Date Received07/10/1987
Decision Date 08/05/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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